Name: rs55668291
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs55668291

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:132628464-132628478 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(G)₉ / del(G)₇ / del(G)₆ / del(…
del(G)₉ / del(G)₇ / del(G)₆ / del(G)₅ / del(G)₄ / delGGG / delGG / delG / dupG / dupGG / dupGGG / dup(G)₄ / dup(G)₅ / dup(G)₆ / dup(G)₇ / dup(G)₈ / dup(G)₉ / dup(G)₁₀ / dup(G)₁₁ / dup(G)₁₂ / dup(G)₁₃ / dup(G)₁₄ / dup(G)₁₅ / ins(G)₁₆ / ins(G)₁₇ / ins(G)₁₈ / ins(G)₁₉ / ins(G)₂₀ / ins(G)₂₁ / ins(G)₂₂
Variation Type: Indel Insertion and Deletion
Frequency: del(G)₉=0.0000 (0/3874, ALFA)
del(G)₆=0.0000 (0/3874, ALFA)
del(G)₅=0.0000 (0/3874, ALFA) (+ 10 more)
del(G)₄=0.0000 (0/3874, ALFA)
delGGG=0.0000 (0/3874, ALFA)
delGG=0.0000 (0/3874, ALFA)
delG=0.0000 (0/3874, ALFA)
dupG=0.0000 (0/3874, ALFA)
dupGG=0.0000 (0/3874, ALFA)
dupGGG=0.0000 (0/3874, ALFA)
dup(G)₄=0.0000 (0/3874, ALFA)
dup(G)₅=0.0000 (0/3874, ALFA)
dupG=0.47 (19/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: INPP5A : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	HWEP
Total	Global	3874	GGGGGGGGGGGGGGG=1.0000	GGGGGG=0.0000, GGGGGGGGG=0.0000, GGGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGGGGG=0.0000	1.0	N/A
European	Sub	2706	GGGGGGGGGGGGGGG=1.0000	GGGGGG=0.0000, GGGGGGGGG=0.0000, GGGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGGGGGG=0.0000	1.0	N/A
African	Sub	726	GGGGGGGGGGGGGGG=1.000	GGGGGG=0.000, GGGGGGGGG=0.000, GGGGGGGGGG=0.000, GGGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGGG=0.000	1.0	N/A
African Others	Sub	28	GGGGGGGGGGGGGGG=1.00	GGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGGGG=0.00	1.0	N/A
African American	Sub	698	GGGGGGGGGGGGGGG=1.000	GGGGGG=0.000, GGGGGGGGG=0.000, GGGGGGGGGG=0.000, GGGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGGG=0.000	1.0	N/A
Asian	Sub	22	GGGGGGGGGGGGGGG=1.00	GGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGGGG=0.00	1.0	N/A
East Asian	Sub	18	GGGGGGGGGGGGGGG=1.00	GGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGGGG=0.00	1.0	N/A
Other Asian	Sub	4	GGGGGGGGGGGGGGG=1.0	GGGGGG=0.0, GGGGGGGGG=0.0, GGGGGGGGGG=0.0, GGGGGGGGGGG=0.0, GGGGGGGGGGGG=0.0, GGGGGGGGGGGGG=0.0, GGGGGGGGGGGGGG=0.0, GGGGGGGGGGGGGGGG=0.0, GGGGGGGGGGGGGGGGG=0.0, GGGGGGGGGGGGGGGGGG=0.0, GGGGGGGGGGGGGGGGGGG=0.0, GGGGGGGGGGGGGGGGGGGG=0.0	1.0	N/A
Latin American 1	Sub	50	GGGGGGGGGGGGGGG=1.00	GGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGGGG=0.00	1.0	N/A
Latin American 2	Sub	222	GGGGGGGGGGGGGGG=1.000	GGGGGG=0.000, GGGGGGGGG=0.000, GGGGGGGGGG=0.000, GGGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGGG=0.000	1.0	N/A
South Asian	Sub	22	GGGGGGGGGGGGGGG=1.00	GGGGGG=0.00, GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGGGGGG=0.00	1.0	N/A
Other	Sub	126	GGGGGGGGGGGGGGG=1.000	GGGGGG=0.000, GGGGGGGGG=0.000, GGGGGGGGGG=0.000, GGGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGGGGGG=0.000	1.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	3874	(G)₁₅=1.0000	del(G)₉=0.0000, del(G)₆=0.0000, del(G)₅=0.0000, del(G)₄=0.0000, delGGG=0.0000, delGG=0.0000, delG=0.0000, dupG=0.0000, dupGG=0.0000, dupGGG=0.0000, dup(G)₄=0.0000, dup(G)₅=0.0000
Allele Frequency Aggregator	European	Sub	2706	(G)₁₅=1.0000	del(G)₉=0.0000, del(G)₆=0.0000, del(G)₅=0.0000, del(G)₄=0.0000, delGGG=0.0000, delGG=0.0000, delG=0.0000, dupG=0.0000, dupGG=0.0000, dupGGG=0.0000, dup(G)₄=0.0000, dup(G)₅=0.0000
Allele Frequency Aggregator	African	Sub	726	(G)₁₅=1.000	del(G)₉=0.000, del(G)₆=0.000, del(G)₅=0.000, del(G)₄=0.000, delGGG=0.000, delGG=0.000, delG=0.000, dupG=0.000, dupGG=0.000, dupGGG=0.000, dup(G)₄=0.000, dup(G)₅=0.000
Allele Frequency Aggregator	Latin American 2	Sub	222	(G)₁₅=1.000	del(G)₉=0.000, del(G)₆=0.000, del(G)₅=0.000, del(G)₄=0.000, delGGG=0.000, delGG=0.000, delG=0.000, dupG=0.000, dupGG=0.000, dupGGG=0.000, dup(G)₄=0.000, dup(G)₅=0.000
Allele Frequency Aggregator	Other	Sub	126	(G)₁₅=1.000	del(G)₉=0.000, del(G)₆=0.000, del(G)₅=0.000, del(G)₄=0.000, delGGG=0.000, delGG=0.000, delG=0.000, dupG=0.000, dupGG=0.000, dupGGG=0.000, dup(G)₄=0.000, dup(G)₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	50	(G)₁₅=1.00	del(G)₉=0.00, del(G)₆=0.00, del(G)₅=0.00, del(G)₄=0.00, delGGG=0.00, delGG=0.00, delG=0.00, dupG=0.00, dupGG=0.00, dupGGG=0.00, dup(G)₄=0.00, dup(G)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	22	(G)₁₅=1.00	del(G)₉=0.00, del(G)₆=0.00, del(G)₅=0.00, del(G)₄=0.00, delGGG=0.00, delGG=0.00, delG=0.00, dupG=0.00, dupGG=0.00, dupGGG=0.00, dup(G)₄=0.00, dup(G)₅=0.00
Allele Frequency Aggregator	Asian	Sub	22	(G)₁₅=1.00	del(G)₉=0.00, del(G)₆=0.00, del(G)₅=0.00, del(G)₄=0.00, delGGG=0.00, delGG=0.00, delG=0.00, dupG=0.00, dupGG=0.00, dupGGG=0.00, dup(G)₄=0.00, dup(G)₅=0.00
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupG=0.47

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 10	NC_000010.11:g.132628470_132628478del
GRCh38.p14 chr 10	NC_000010.11:g.132628472_132628478del
GRCh38.p14 chr 10	NC_000010.11:g.132628473_132628478del
GRCh38.p14 chr 10	NC_000010.11:g.132628474_132628478del
GRCh38.p14 chr 10	NC_000010.11:g.132628475_132628478del
GRCh38.p14 chr 10	NC_000010.11:g.132628476_132628478del
GRCh38.p14 chr 10	NC_000010.11:g.132628477_132628478del
GRCh38.p14 chr 10	NC_000010.11:g.132628478del
GRCh38.p14 chr 10	NC_000010.11:g.132628478dup
GRCh38.p14 chr 10	NC_000010.11:g.132628477_132628478dup
GRCh38.p14 chr 10	NC_000010.11:g.132628476_132628478dup
GRCh38.p14 chr 10	NC_000010.11:g.132628475_132628478dup
GRCh38.p14 chr 10	NC_000010.11:g.132628474_132628478dup
GRCh38.p14 chr 10	NC_000010.11:g.132628473_132628478dup
GRCh38.p14 chr 10	NC_000010.11:g.132628472_132628478dup
GRCh38.p14 chr 10	NC_000010.11:g.132628471_132628478dup
GRCh38.p14 chr 10	NC_000010.11:g.132628470_132628478dup
GRCh38.p14 chr 10	NC_000010.11:g.132628469_132628478dup
GRCh38.p14 chr 10	NC_000010.11:g.132628468_132628478dup
GRCh38.p14 chr 10	NC_000010.11:g.132628467_132628478dup
GRCh38.p14 chr 10	NC_000010.11:g.132628466_132628478dup
GRCh38.p14 chr 10	NC_000010.11:g.132628465_132628478dup
GRCh38.p14 chr 10	NC_000010.11:g.132628464_132628478dup
GRCh38.p14 chr 10	NC_000010.11:g.132628478_132628479insGGGGGGGGGGGGGGGG
GRCh38.p14 chr 10	NC_000010.11:g.132628478_132628479insGGGGGGGGGGGGGGGGG
GRCh38.p14 chr 10	NC_000010.11:g.132628478_132628479insGGGGGGGGGGGGGGGGGG
GRCh38.p14 chr 10	NC_000010.11:g.132628478_132628479insGGGGGGGGGGGGGGGGGGG
GRCh38.p14 chr 10	NC_000010.11:g.132628478_132628479insGGGGGGGGGGGGGGGGGGGG
GRCh38.p14 chr 10	NC_000010.11:g.132628478_132628479insGGGGGGGGGGGGGGGGGGGGG
GRCh38.p14 chr 10	NC_000010.11:g.132628478_132628479insGGGGGGGGGGGGGGGGGGGGGG
GRCh37.p13 chr 10	NC_000010.10:g.134441974_134441982del
GRCh37.p13 chr 10	NC_000010.10:g.134441976_134441982del
GRCh37.p13 chr 10	NC_000010.10:g.134441977_134441982del
GRCh37.p13 chr 10	NC_000010.10:g.134441978_134441982del
GRCh37.p13 chr 10	NC_000010.10:g.134441979_134441982del
GRCh37.p13 chr 10	NC_000010.10:g.134441980_134441982del
GRCh37.p13 chr 10	NC_000010.10:g.134441981_134441982del
GRCh37.p13 chr 10	NC_000010.10:g.134441982del
GRCh37.p13 chr 10	NC_000010.10:g.134441982dup
GRCh37.p13 chr 10	NC_000010.10:g.134441981_134441982dup
GRCh37.p13 chr 10	NC_000010.10:g.134441980_134441982dup
GRCh37.p13 chr 10	NC_000010.10:g.134441979_134441982dup
GRCh37.p13 chr 10	NC_000010.10:g.134441978_134441982dup
GRCh37.p13 chr 10	NC_000010.10:g.134441977_134441982dup
GRCh37.p13 chr 10	NC_000010.10:g.134441976_134441982dup
GRCh37.p13 chr 10	NC_000010.10:g.134441975_134441982dup
GRCh37.p13 chr 10	NC_000010.10:g.134441974_134441982dup
GRCh37.p13 chr 10	NC_000010.10:g.134441973_134441982dup
GRCh37.p13 chr 10	NC_000010.10:g.134441972_134441982dup
GRCh37.p13 chr 10	NC_000010.10:g.134441971_134441982dup
GRCh37.p13 chr 10	NC_000010.10:g.134441970_134441982dup
GRCh37.p13 chr 10	NC_000010.10:g.134441969_134441982dup
GRCh37.p13 chr 10	NC_000010.10:g.134441968_134441982dup
GRCh37.p13 chr 10	NC_000010.10:g.134441982_134441983insGGGGGGGGGGGGGGGG
GRCh37.p13 chr 10	NC_000010.10:g.134441982_134441983insGGGGGGGGGGGGGGGGG
GRCh37.p13 chr 10	NC_000010.10:g.134441982_134441983insGGGGGGGGGGGGGGGGGG
GRCh37.p13 chr 10	NC_000010.10:g.134441982_134441983insGGGGGGGGGGGGGGGGGGG
GRCh37.p13 chr 10	NC_000010.10:g.134441982_134441983insGGGGGGGGGGGGGGGGGGGG
GRCh37.p13 chr 10	NC_000010.10:g.134441982_134441983insGGGGGGGGGGGGGGGGGGGGG
GRCh37.p13 chr 10	NC_000010.10:g.134441982_134441983insGGGGGGGGGGGGGGGGGGGGGG
LOC110121444 genomic region	NG_054057.1:g.46_54del
LOC110121444 genomic region	NG_054057.1:g.48_54del
LOC110121444 genomic region	NG_054057.1:g.49_54del
LOC110121444 genomic region	NG_054057.1:g.50_54del
LOC110121444 genomic region	NG_054057.1:g.51_54del
LOC110121444 genomic region	NG_054057.1:g.52_54del
LOC110121444 genomic region	NG_054057.1:g.53_54del
LOC110121444 genomic region	NG_054057.1:g.54del
LOC110121444 genomic region	NG_054057.1:g.54dup
LOC110121444 genomic region	NG_054057.1:g.53_54dup
LOC110121444 genomic region	NG_054057.1:g.52_54dup
LOC110121444 genomic region	NG_054057.1:g.51_54dup
LOC110121444 genomic region	NG_054057.1:g.50_54dup
LOC110121444 genomic region	NG_054057.1:g.49_54dup
LOC110121444 genomic region	NG_054057.1:g.48_54dup
LOC110121444 genomic region	NG_054057.1:g.47_54dup
LOC110121444 genomic region	NG_054057.1:g.46_54dup
LOC110121444 genomic region	NG_054057.1:g.45_54dup
LOC110121444 genomic region	NG_054057.1:g.44_54dup
LOC110121444 genomic region	NG_054057.1:g.43_54dup
LOC110121444 genomic region	NG_054057.1:g.42_54dup
LOC110121444 genomic region	NG_054057.1:g.41_54dup
LOC110121444 genomic region	NG_054057.1:g.40_54dup
LOC110121444 genomic region	NG_054057.1:g.54_55insGGGGGGGGGGGGGGGG
LOC110121444 genomic region	NG_054057.1:g.54_55insGGGGGGGGGGGGGGGGG
LOC110121444 genomic region	NG_054057.1:g.54_55insGGGGGGGGGGGGGGGGGG
LOC110121444 genomic region	NG_054057.1:g.54_55insGGGGGGGGGGGGGGGGGGG
LOC110121444 genomic region	NG_054057.1:g.54_55insGGGGGGGGGGGGGGGGGGGG
LOC110121444 genomic region	NG_054057.1:g.54_55insGGGGGGGGGGGGGGGGGGGGG
LOC110121444 genomic region	NG_054057.1:g.54_55insGGGGGGGGGGGGGGGGGGGGGG

Gene: INPP5A, inositol polyphosphate-5-phosphatase A (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
INPP5A transcript variant 1	NM_005539.5:c.118-17398_1… NM_005539.5:c.118-17398_118-17390del	N/A	Intron Variant
INPP5A transcript variant 2	NM_001321042.2:c.	N/A	Genic Upstream Transcript Variant
INPP5A transcript variant X3	XM_017016205.2:c.118-1739… XM_017016205.2:c.118-17398_118-17390del	N/A	Intron Variant
INPP5A transcript variant X1	XM_017016204.2:c.	N/A	Genic Upstream Transcript Variant
INPP5A transcript variant X5	XR_001747104.2:n.	N/A	Intron Variant
INPP5A transcript variant X2	XR_007061962.1:n.	N/A	Intron Variant
INPP5A transcript variant X6	XR_007061963.1:n.	N/A	Intron Variant
INPP5A transcript variant X4	XR_945735.2:n.	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(G)₁₅=	del(G)₉	del(G)₇	del(G)₆	del(G)₅	del(G)₄	delGGG	delGG	delG	dupG	dupGG	dupGGG	dup(G)₄	dup(G)₅	dup(G)₆	dup(G)₇	dup(G)₈	dup(G)₉	dup(G)₁₀	dup(G)₁₁	dup(G)₁₂	dup(G)₁₃	dup(G)₁₄	dup(G)₁₅	ins(G)₁₆	ins(G)₁₇	ins(G)₁₈	ins(G)₁₉	ins(G)₂₀	ins(G)₂₁	ins(G)₂₂
GRCh38.p14 chr 10	NC_000010.11:g.132628464_132628478=	NC_000010.11:g.132628470_132628478del	NC_000010.11:g.132628472_132628478del	NC_000010.11:g.132628473_132628478del	NC_000010.11:g.132628474_132628478del	NC_000010.11:g.132628475_132628478del	NC_000010.11:g.132628476_132628478del	NC_000010.11:g.132628477_132628478del	NC_000010.11:g.132628478del	NC_000010.11:g.132628478dup	NC_000010.11:g.132628477_132628478dup	NC_000010.11:g.132628476_132628478dup	NC_000010.11:g.132628475_132628478dup	NC_000010.11:g.132628474_132628478dup	NC_000010.11:g.132628473_132628478dup	NC_000010.11:g.132628472_132628478dup	NC_000010.11:g.132628471_132628478dup	NC_000010.11:g.132628470_132628478dup	NC_000010.11:g.132628469_132628478dup	NC_000010.11:g.132628468_132628478dup	NC_000010.11:g.132628467_132628478dup	NC_000010.11:g.132628466_132628478dup	NC_000010.11:g.132628465_132628478dup	NC_000010.11:g.132628464_132628478dup	NC_000010.11:g.132628478_132628479insGGGGGGGGGGGGGGGG	NC_000010.11:g.132628478_132628479insGGGGGGGGGGGGGGGGG	NC_000010.11:g.132628478_132628479insGGGGGGGGGGGGGGGGGG	NC_000010.11:g.132628478_132628479insGGGGGGGGGGGGGGGGGGG	NC_000010.11:g.132628478_132628479insGGGGGGGGGGGGGGGGGGGG	NC_000010.11:g.132628478_132628479insGGGGGGGGGGGGGGGGGGGGG	NC_000010.11:g.132628478_132628479insGGGGGGGGGGGGGGGGGGGGGG
GRCh37.p13 chr 10	NC_000010.10:g.134441968_134441982=	NC_000010.10:g.134441974_134441982del	NC_000010.10:g.134441976_134441982del	NC_000010.10:g.134441977_134441982del	NC_000010.10:g.134441978_134441982del	NC_000010.10:g.134441979_134441982del	NC_000010.10:g.134441980_134441982del	NC_000010.10:g.134441981_134441982del	NC_000010.10:g.134441982del	NC_000010.10:g.134441982dup	NC_000010.10:g.134441981_134441982dup	NC_000010.10:g.134441980_134441982dup	NC_000010.10:g.134441979_134441982dup	NC_000010.10:g.134441978_134441982dup	NC_000010.10:g.134441977_134441982dup	NC_000010.10:g.134441976_134441982dup	NC_000010.10:g.134441975_134441982dup	NC_000010.10:g.134441974_134441982dup	NC_000010.10:g.134441973_134441982dup	NC_000010.10:g.134441972_134441982dup	NC_000010.10:g.134441971_134441982dup	NC_000010.10:g.134441970_134441982dup	NC_000010.10:g.134441969_134441982dup	NC_000010.10:g.134441968_134441982dup	NC_000010.10:g.134441982_134441983insGGGGGGGGGGGGGGGG	NC_000010.10:g.134441982_134441983insGGGGGGGGGGGGGGGGG	NC_000010.10:g.134441982_134441983insGGGGGGGGGGGGGGGGGG	NC_000010.10:g.134441982_134441983insGGGGGGGGGGGGGGGGGGG	NC_000010.10:g.134441982_134441983insGGGGGGGGGGGGGGGGGGGG	NC_000010.10:g.134441982_134441983insGGGGGGGGGGGGGGGGGGGGG	NC_000010.10:g.134441982_134441983insGGGGGGGGGGGGGGGGGGGGGG
LOC110121444 genomic region	NG_054057.1:g.40_54=	NG_054057.1:g.46_54del	NG_054057.1:g.48_54del	NG_054057.1:g.49_54del	NG_054057.1:g.50_54del	NG_054057.1:g.51_54del	NG_054057.1:g.52_54del	NG_054057.1:g.53_54del	NG_054057.1:g.54del	NG_054057.1:g.54dup	NG_054057.1:g.53_54dup	NG_054057.1:g.52_54dup	NG_054057.1:g.51_54dup	NG_054057.1:g.50_54dup	NG_054057.1:g.49_54dup	NG_054057.1:g.48_54dup	NG_054057.1:g.47_54dup	NG_054057.1:g.46_54dup	NG_054057.1:g.45_54dup	NG_054057.1:g.44_54dup	NG_054057.1:g.43_54dup	NG_054057.1:g.42_54dup	NG_054057.1:g.41_54dup	NG_054057.1:g.40_54dup	NG_054057.1:g.54_55insGGGGGGGGGGGGGGGG	NG_054057.1:g.54_55insGGGGGGGGGGGGGGGGG	NG_054057.1:g.54_55insGGGGGGGGGGGGGGGGGG	NG_054057.1:g.54_55insGGGGGGGGGGGGGGGGGGG	NG_054057.1:g.54_55insGGGGGGGGGGGGGGGGGGGG	NG_054057.1:g.54_55insGGGGGGGGGGGGGGGGGGGGG	NG_054057.1:g.54_55insGGGGGGGGGGGGGGGGGGGGGG
INPP5A transcript	NM_005539.3:c.118-17404=	NM_005539.3:c.118-17398_118-17390del	NM_005539.3:c.118-17396_118-17390del	NM_005539.3:c.118-17395_118-17390del	NM_005539.3:c.118-17394_118-17390del	NM_005539.3:c.118-17393_118-17390del	NM_005539.3:c.118-17392_118-17390del	NM_005539.3:c.118-17391_118-17390del	NM_005539.3:c.118-17390del	NM_005539.3:c.118-17390dup	NM_005539.3:c.118-17391_118-17390dup	NM_005539.3:c.118-17392_118-17390dup	NM_005539.3:c.118-17393_118-17390dup	NM_005539.3:c.118-17394_118-17390dup	NM_005539.3:c.118-17395_118-17390dup	NM_005539.3:c.118-17396_118-17390dup	NM_005539.3:c.118-17397_118-17390dup	NM_005539.3:c.118-17398_118-17390dup	NM_005539.3:c.118-17399_118-17390dup	NM_005539.3:c.118-17400_118-17390dup	NM_005539.3:c.118-17401_118-17390dup	NM_005539.3:c.118-17402_118-17390dup	NM_005539.3:c.118-17403_118-17390dup	NM_005539.3:c.118-17404_118-17390dup	NM_005539.3:c.118-17390_118-17389insGGGGGGGGGGGGGGGG	NM_005539.3:c.118-17390_118-17389insGGGGGGGGGGGGGGGGG	NM_005539.3:c.118-17390_118-17389insGGGGGGGGGGGGGGGGGG	NM_005539.3:c.118-17390_118-17389insGGGGGGGGGGGGGGGGGGG	NM_005539.3:c.118-17390_118-17389insGGGGGGGGGGGGGGGGGGGG	NM_005539.3:c.118-17390_118-17389insGGGGGGGGGGGGGGGGGGGGG	NM_005539.3:c.118-17390_118-17389insGGGGGGGGGGGGGGGGGGGGGG
INPP5A transcript variant 1	NM_005539.5:c.118-17404=	NM_005539.5:c.118-17398_118-17390del	NM_005539.5:c.118-17396_118-17390del	NM_005539.5:c.118-17395_118-17390del	NM_005539.5:c.118-17394_118-17390del	NM_005539.5:c.118-17393_118-17390del	NM_005539.5:c.118-17392_118-17390del	NM_005539.5:c.118-17391_118-17390del	NM_005539.5:c.118-17390del	NM_005539.5:c.118-17390dup	NM_005539.5:c.118-17391_118-17390dup	NM_005539.5:c.118-17392_118-17390dup	NM_005539.5:c.118-17393_118-17390dup	NM_005539.5:c.118-17394_118-17390dup	NM_005539.5:c.118-17395_118-17390dup	NM_005539.5:c.118-17396_118-17390dup	NM_005539.5:c.118-17397_118-17390dup	NM_005539.5:c.118-17398_118-17390dup	NM_005539.5:c.118-17399_118-17390dup	NM_005539.5:c.118-17400_118-17390dup	NM_005539.5:c.118-17401_118-17390dup	NM_005539.5:c.118-17402_118-17390dup	NM_005539.5:c.118-17403_118-17390dup	NM_005539.5:c.118-17404_118-17390dup	NM_005539.5:c.118-17390_118-17389insGGGGGGGGGGGGGGGG	NM_005539.5:c.118-17390_118-17389insGGGGGGGGGGGGGGGGG	NM_005539.5:c.118-17390_118-17389insGGGGGGGGGGGGGGGGGG	NM_005539.5:c.118-17390_118-17389insGGGGGGGGGGGGGGGGGGG	NM_005539.5:c.118-17390_118-17389insGGGGGGGGGGGGGGGGGGGG	NM_005539.5:c.118-17390_118-17389insGGGGGGGGGGGGGGGGGGGGG	NM_005539.5:c.118-17390_118-17389insGGGGGGGGGGGGGGGGGGGGGG
INPP5A transcript variant X1	XM_005252681.1:c.118-17404=	XM_005252681.1:c.118-17398_118-17390del	XM_005252681.1:c.118-17396_118-17390del	XM_005252681.1:c.118-17395_118-17390del	XM_005252681.1:c.118-17394_118-17390del	XM_005252681.1:c.118-17393_118-17390del	XM_005252681.1:c.118-17392_118-17390del	XM_005252681.1:c.118-17391_118-17390del	XM_005252681.1:c.118-17390del	XM_005252681.1:c.118-17390dup	XM_005252681.1:c.118-17391_118-17390dup	XM_005252681.1:c.118-17392_118-17390dup	XM_005252681.1:c.118-17393_118-17390dup	XM_005252681.1:c.118-17394_118-17390dup	XM_005252681.1:c.118-17395_118-17390dup	XM_005252681.1:c.118-17396_118-17390dup	XM_005252681.1:c.118-17397_118-17390dup	XM_005252681.1:c.118-17398_118-17390dup	XM_005252681.1:c.118-17399_118-17390dup	XM_005252681.1:c.118-17400_118-17390dup	XM_005252681.1:c.118-17401_118-17390dup	XM_005252681.1:c.118-17402_118-17390dup	XM_005252681.1:c.118-17403_118-17390dup	XM_005252681.1:c.118-17404_118-17390dup	XM_005252681.1:c.118-17390_118-17389insGGGGGGGGGGGGGGGG	XM_005252681.1:c.118-17390_118-17389insGGGGGGGGGGGGGGGGG	XM_005252681.1:c.118-17390_118-17389insGGGGGGGGGGGGGGGGGG	XM_005252681.1:c.118-17390_118-17389insGGGGGGGGGGGGGGGGGGG	XM_005252681.1:c.118-17390_118-17389insGGGGGGGGGGGGGGGGGGGG	XM_005252681.1:c.118-17390_118-17389insGGGGGGGGGGGGGGGGGGGGG	XM_005252681.1:c.118-17390_118-17389insGGGGGGGGGGGGGGGGGGGGGG
INPP5A transcript variant X3	XM_017016205.2:c.118-17404=	XM_017016205.2:c.118-17398_118-17390del	XM_017016205.2:c.118-17396_118-17390del	XM_017016205.2:c.118-17395_118-17390del	XM_017016205.2:c.118-17394_118-17390del	XM_017016205.2:c.118-17393_118-17390del	XM_017016205.2:c.118-17392_118-17390del	XM_017016205.2:c.118-17391_118-17390del	XM_017016205.2:c.118-17390del	XM_017016205.2:c.118-17390dup	XM_017016205.2:c.118-17391_118-17390dup	XM_017016205.2:c.118-17392_118-17390dup	XM_017016205.2:c.118-17393_118-17390dup	XM_017016205.2:c.118-17394_118-17390dup	XM_017016205.2:c.118-17395_118-17390dup	XM_017016205.2:c.118-17396_118-17390dup	XM_017016205.2:c.118-17397_118-17390dup	XM_017016205.2:c.118-17398_118-17390dup	XM_017016205.2:c.118-17399_118-17390dup	XM_017016205.2:c.118-17400_118-17390dup	XM_017016205.2:c.118-17401_118-17390dup	XM_017016205.2:c.118-17402_118-17390dup	XM_017016205.2:c.118-17403_118-17390dup	XM_017016205.2:c.118-17404_118-17390dup	XM_017016205.2:c.118-17390_118-17389insGGGGGGGGGGGGGGGG	XM_017016205.2:c.118-17390_118-17389insGGGGGGGGGGGGGGGGG	XM_017016205.2:c.118-17390_118-17389insGGGGGGGGGGGGGGGGGG	XM_017016205.2:c.118-17390_118-17389insGGGGGGGGGGGGGGGGGGG	XM_017016205.2:c.118-17390_118-17389insGGGGGGGGGGGGGGGGGGGG	XM_017016205.2:c.118-17390_118-17389insGGGGGGGGGGGGGGGGGGGGG	XM_017016205.2:c.118-17390_118-17389insGGGGGGGGGGGGGGGGGGGGGG

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

61 SubSNP, 40 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss77959292	Dec 06, 2007 (129)
2	HGSV	ss80461982	Dec 14, 2007 (130)
3	PJP	ss294684682	May 09, 2011 (134)
4	SSMP	ss663965438	Apr 01, 2015 (144)
5	SSIP	ss947269848	Aug 21, 2014 (142)
6	EVA_GENOME_DK	ss1574284541	Apr 01, 2015 (144)
7	SWEGEN	ss3007418800	Nov 08, 2017 (151)
8	MCHAISSO	ss3063676223	Jan 10, 2018 (151)
9	EVA_DECODE	ss3691019079	Jul 13, 2019 (153)
10	EVA_DECODE	ss3691019080	Jul 13, 2019 (153)
11	EVA_DECODE	ss3691019081	Jul 13, 2019 (153)
12	EVA_DECODE	ss3691019082	Jul 13, 2019 (153)
13	EVA_DECODE	ss3691019083	Jul 13, 2019 (153)
14	EVA_DECODE	ss3691019084	Jul 13, 2019 (153)
15	PACBIO	ss3786834784	Jul 13, 2019 (153)
16	PACBIO	ss3791991163	Jul 13, 2019 (153)
17	PACBIO	ss3791991164	Jul 13, 2019 (153)
18	PACBIO	ss3796873355	Jul 13, 2019 (153)
19	PACBIO	ss3796873356	Jul 13, 2019 (153)
20	EVA	ss3832422841	Apr 26, 2020 (154)
21	GNOMAD	ss4228465185	Apr 26, 2021 (155)
22	GNOMAD	ss4228465186	Apr 26, 2021 (155)
23	GNOMAD	ss4228465187	Apr 26, 2021 (155)
24	GNOMAD	ss4228465188	Apr 26, 2021 (155)
25	GNOMAD	ss4228465189	Apr 26, 2021 (155)
26	GNOMAD	ss4228465190	Apr 26, 2021 (155)
27	GNOMAD	ss4228465191	Apr 26, 2021 (155)
28	GNOMAD	ss4228465192	Apr 26, 2021 (155)
29	GNOMAD	ss4228465193	Apr 26, 2021 (155)
30	GNOMAD	ss4228465194	Apr 26, 2021 (155)
31	GNOMAD	ss4228465195	Apr 26, 2021 (155)
32	GNOMAD	ss4228465196	Apr 26, 2021 (155)
33	GNOMAD	ss4228465197	Apr 26, 2021 (155)
34	GNOMAD	ss4228465198	Apr 26, 2021 (155)
35	GNOMAD	ss4228465199	Apr 26, 2021 (155)
36	GNOMAD	ss4228465200	Apr 26, 2021 (155)
37	GNOMAD	ss4228465201	Apr 26, 2021 (155)
38	GNOMAD	ss4228465202	Apr 26, 2021 (155)
39	GNOMAD	ss4228465203	Apr 26, 2021 (155)
40	GNOMAD	ss4228465204	Apr 26, 2021 (155)
41	GNOMAD	ss4228465205	Apr 26, 2021 (155)
42	GNOMAD	ss4228465206	Apr 26, 2021 (155)
43	GNOMAD	ss4228465207	Apr 26, 2021 (155)
44	GNOMAD	ss4228465208	Apr 26, 2021 (155)
45	GNOMAD	ss4228465209	Apr 26, 2021 (155)
46	GNOMAD	ss4228465210	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5200217389	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5200217390	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5200217391	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5200217392	Apr 26, 2021 (155)
51	TOMMO_GENOMICS	ss5200217393	Apr 26, 2021 (155)
52	TOMMO_GENOMICS	ss5200217394	Apr 26, 2021 (155)
53	HUGCELL_USP	ss5481415451	Oct 16, 2022 (156)
54	HUGCELL_USP	ss5481415452	Oct 16, 2022 (156)
55	HUGCELL_USP	ss5481415453	Oct 16, 2022 (156)
56	TOMMO_GENOMICS	ss5746822212	Oct 16, 2022 (156)
57	TOMMO_GENOMICS	ss5746822213	Oct 16, 2022 (156)
58	TOMMO_GENOMICS	ss5746822214	Oct 16, 2022 (156)
59	TOMMO_GENOMICS	ss5746822215	Oct 16, 2022 (156)
60	TOMMO_GENOMICS	ss5746822216	Oct 16, 2022 (156)
61	TOMMO_GENOMICS	ss5746822217	Oct 16, 2022 (156)
62	The Danish reference pan genome	NC_000010.10 - 134441968	Apr 26, 2020 (154)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 368632926 (NC_000010.11:132628463::G 21/20960) Row 368632927 (NC_000010.11:132628463::GG 6/20966) Row 368632928 (NC_000010.11:132628463::GGGGG 13/20970)...	-	Apr 26, 2021 (155)
89	8.3KJPN Submission ignored due to conflicting rows: Row 58186696 (NC_000010.10:134441967:GGG: 1102/9468) Row 58186697 (NC_000010.10:134441967:G: 2612/9468) Row 58186698 (NC_000010.10:134441967::GGGGGGGGGGGGGGGG 574/9468)...	-	Apr 26, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 58186696 (NC_000010.10:134441967:GGG: 1102/9468) Row 58186697 (NC_000010.10:134441967:G: 2612/9468) Row 58186698 (NC_000010.10:134441967::GGGGGGGGGGGGGGGG 574/9468)...	-	Apr 26, 2021 (155)
91	8.3KJPN Submission ignored due to conflicting rows: Row 58186696 (NC_000010.10:134441967:GGG: 1102/9468) Row 58186697 (NC_000010.10:134441967:G: 2612/9468) Row 58186698 (NC_000010.10:134441967::GGGGGGGGGGGGGGGG 574/9468)...	-	Apr 26, 2021 (155)
92	8.3KJPN Submission ignored due to conflicting rows: Row 58186696 (NC_000010.10:134441967:GGG: 1102/9468) Row 58186697 (NC_000010.10:134441967:G: 2612/9468) Row 58186698 (NC_000010.10:134441967::GGGGGGGGGGGGGGGG 574/9468)...	-	Apr 26, 2021 (155)
93	8.3KJPN Submission ignored due to conflicting rows: Row 58186696 (NC_000010.10:134441967:GGG: 1102/9468) Row 58186697 (NC_000010.10:134441967:G: 2612/9468) Row 58186698 (NC_000010.10:134441967::GGGGGGGGGGGGGGGG 574/9468)...	-	Apr 26, 2021 (155)
94	8.3KJPN Submission ignored due to conflicting rows: Row 58186696 (NC_000010.10:134441967:GGG: 1102/9468) Row 58186697 (NC_000010.10:134441967:G: 2612/9468) Row 58186698 (NC_000010.10:134441967::GGGGGGGGGGGGGGGG 574/9468)...	-	Apr 26, 2021 (155)
95	14KJPN Submission ignored due to conflicting rows: Row 80659316 (NC_000010.11:132628463:GGG: 1945/21374) Row 80659317 (NC_000010.11:132628463:G: 5991/21374) Row 80659318 (NC_000010.11:132628463::GGGGGGGGGGGGGGGG 575/21374)...	-	Oct 16, 2022 (156)
96	14KJPN Submission ignored due to conflicting rows: Row 80659316 (NC_000010.11:132628463:GGG: 1945/21374) Row 80659317 (NC_000010.11:132628463:G: 5991/21374) Row 80659318 (NC_000010.11:132628463::GGGGGGGGGGGGGGGG 575/21374)...	-	Oct 16, 2022 (156)
97	14KJPN Submission ignored due to conflicting rows: Row 80659316 (NC_000010.11:132628463:GGG: 1945/21374) Row 80659317 (NC_000010.11:132628463:G: 5991/21374) Row 80659318 (NC_000010.11:132628463::GGGGGGGGGGGGGGGG 575/21374)...	-	Oct 16, 2022 (156)
98	14KJPN Submission ignored due to conflicting rows: Row 80659316 (NC_000010.11:132628463:GGG: 1945/21374) Row 80659317 (NC_000010.11:132628463:G: 5991/21374) Row 80659318 (NC_000010.11:132628463::GGGGGGGGGGGGGGGG 575/21374)...	-	Oct 16, 2022 (156)
99	14KJPN Submission ignored due to conflicting rows: Row 80659316 (NC_000010.11:132628463:GGG: 1945/21374) Row 80659317 (NC_000010.11:132628463:G: 5991/21374) Row 80659318 (NC_000010.11:132628463::GGGGGGGGGGGGGGGG 575/21374)...	-	Oct 16, 2022 (156)
100	14KJPN Submission ignored due to conflicting rows: Row 80659316 (NC_000010.11:132628463:GGG: 1945/21374) Row 80659317 (NC_000010.11:132628463:G: 5991/21374) Row 80659318 (NC_000010.11:132628463::GGGGGGGGGGGGGGGG 575/21374)...	-	Oct 16, 2022 (156)
101	ALFA	NC_000010.11 - 132628464	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs57381511	May 23, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4228465210	NC_000010.11:132628463:GGGGGGGGG:	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGG	(self)
5229021768	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGG	(self)
ss4228465209	NC_000010.11:132628463:GGGGGGG:	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGG	(self)
ss4228465208	NC_000010.11:132628463:GGGGGG:	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGG	(self)
5229021768	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGG	(self)
5229021768	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGG	(self)
ss4228465207	NC_000010.11:132628463:GGGG:	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGG	(self)
5229021768	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGG	(self)
ss663965438, ss947269848, ss3007418800, ss5200217389	NC_000010.10:134441967:GGG:	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGG	(self)
ss3691019084, ss5481415452, ss5746822212	NC_000010.11:132628463:GGG:	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGG	(self)
5229021768	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGG	(self)
ss3832422841	NC_000010.10:134441967:GG:	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGG	(self)
ss3063676223, ss4228465206, ss5481415451	NC_000010.11:132628463:GG:	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGG	(self)
5229021768	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGG	(self)
ss3691019083	NC_000010.11:132628464:GG:	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGG	(self)
ss77959292, ss80461982	NC_000010.8:134291971:G:	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGG	(self)
ss294684682	NC_000010.9:134291971:G:	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGG	(self)
ss3791991163, ss3796873355, ss5200217390	NC_000010.10:134441967:G:	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGG	(self)
ss4228465205, ss5481415453, ss5746822213	NC_000010.11:132628463:G:	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGG	(self)
5229021768	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGG	(self)
ss3691019082	NC_000010.11:132628465:G:	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGG	(self)
273886, ss1574284541	NC_000010.10:134441967::G	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGG	(self)
ss4228465185, ss5746822215	NC_000010.11:132628463::G	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGG	(self)
5229021768	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGG	(self)
ss3691019081	NC_000010.11:132628466::G	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGG	(self)
ss5200217393	NC_000010.10:134441967::GG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGG	(self)
ss4228465186, ss5746822217	NC_000010.11:132628463::GG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGG	(self)
5229021768	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGG	(self)
ss3691019080	NC_000010.11:132628466::GG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGG	(self)
ss3786834784, ss3791991164, ss3796873356	NC_000010.10:134441967::GGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGG	(self)
5229021768	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGG	(self)
5229021768	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGG	(self)
ss3691019079	NC_000010.11:132628466::GGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGG	(self)
ss4228465187	NC_000010.11:132628463::GGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGG	(self)
5229021768	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGG	(self)
ss4228465188	NC_000010.11:132628463::GGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGG	(self)
ss4228465189	NC_000010.11:132628463::GGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGG	(self)
ss4228465190	NC_000010.11:132628463::GGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGG	(self)
ss4228465191	NC_000010.11:132628463::GGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss4228465192	NC_000010.11:132628463::GGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss4228465193	NC_000010.11:132628463::GGGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss4228465194	NC_000010.11:132628463::GGGGGGGGGG… NC_000010.11:132628463::GGGGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss4228465195	NC_000010.11:132628463::GGGGGGGGGG… NC_000010.11:132628463::GGGGGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss4228465196	NC_000010.11:132628463::GGGGGGGGGG… NC_000010.11:132628463::GGGGGGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss5200217392	NC_000010.10:134441967::GGGGGGGGGG… NC_000010.10:134441967::GGGGGGGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss4228465197, ss5746822216	NC_000010.11:132628463::GGGGGGGGGG… NC_000010.11:132628463::GGGGGGGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss5200217391	NC_000010.10:134441967::GGGGGGGGGG… NC_000010.10:134441967::GGGGGGGGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss4228465198, ss5746822214	NC_000010.11:132628463::GGGGGGGGGG… NC_000010.11:132628463::GGGGGGGGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss5200217394	NC_000010.10:134441967::GGGGGGGGGG… NC_000010.10:134441967::GGGGGGGGGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss4228465199	NC_000010.11:132628463::GGGGGGGGGG… NC_000010.11:132628463::GGGGGGGGGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss4228465200	NC_000010.11:132628463::GGGGGGGGGG… NC_000010.11:132628463::GGGGGGGGGGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss4228465201	NC_000010.11:132628463::GGGGGGGGGG… NC_000010.11:132628463::GGGGGGGGGGGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss4228465202	NC_000010.11:132628463::GGGGGGGGGG… NC_000010.11:132628463::GGGGGGGGGGGGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss4228465203	NC_000010.11:132628463::GGGGGGGGGG… NC_000010.11:132628463::GGGGGGGGGGGGGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	(self)
ss4228465204	NC_000010.11:132628463::GGGGGGGGGG… NC_000010.11:132628463::GGGGGGGGGGGGGGGGGGGGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI
ss3134602478	NC_000010.11:132628463::GGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGG
ss3134602479	NC_000010.11:132628463::GGGG	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGG
ss3134602486	NC_000010.11:132628463:GGGGG:	NC_000010.11:132628463:GGGGGGGGGGG… NC_000010.11:132628463:GGGGGGGGGGGGGGG:GGGGGGGGGG

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs55668291

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs55668291