Name: rs56820180
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.

rs56820180

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:126446149-126446170 (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(A)₈ / del(A)₇ / del(A)₄ / delA…
del(A)₈ / del(A)₇ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₁₀ / dup(A)₁₈ / dup(A)₂₂
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₈=0.000 (0/850, ALFA)
del(A)₇=0.000 (0/850, ALFA)
del(A)₄=0.000 (0/850, ALFA) (+ 9 more)
delAAA=0.000 (0/850, ALFA)
delAA=0.000 (0/850, ALFA)
delA=0.000 (0/850, ALFA)
dupA=0.000 (0/850, ALFA)
dupAA=0.000 (0/850, ALFA)
dupAAA=0.000 (0/850, ALFA)
dup(A)₄=0.000 (0/850, ALFA)
dup(A)₅=0.000 (0/850, ALFA)
delA=0.38 (15/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: KIRREL3 : 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	850	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
European	Sub	462	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African	Sub	222	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	14	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	208	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	20	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	12	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	8	AAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	8	AAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 2	Sub	70	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
South Asian	Sub	20	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	48	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	850	(A)₂₂=1.000	del(A)₈=0.000, del(A)₇=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	European	Sub	462	(A)₂₂=1.000	del(A)₈=0.000, del(A)₇=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	African	Sub	222	(A)₂₂=1.000	del(A)₈=0.000, del(A)₇=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Latin American 2	Sub	70	(A)₂₂=1.00	del(A)₈=0.00, del(A)₇=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Other	Sub	48	(A)₂₂=1.00	del(A)₈=0.00, del(A)₇=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	20	(A)₂₂=1.00	del(A)₈=0.00, del(A)₇=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Asian	Sub	20	(A)₂₂=1.00	del(A)₈=0.00, del(A)₇=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Latin American 1	Sub	8	(A)₂₂=1.0	del(A)₈=0.0, del(A)₇=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0, dup(A)₅=0.0
The Danish reference pan genome	Danish	Study-wide	40	(A)₂₂=0.62	delA=0.38

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 11	NC_000011.10:g.126446163_126446170del
GRCh38.p14 chr 11	NC_000011.10:g.126446164_126446170del
GRCh38.p14 chr 11	NC_000011.10:g.126446167_126446170del
GRCh38.p14 chr 11	NC_000011.10:g.126446168_126446170del
GRCh38.p14 chr 11	NC_000011.10:g.126446169_126446170del
GRCh38.p14 chr 11	NC_000011.10:g.126446170del
GRCh38.p14 chr 11	NC_000011.10:g.126446170dup
GRCh38.p14 chr 11	NC_000011.10:g.126446169_126446170dup
GRCh38.p14 chr 11	NC_000011.10:g.126446168_126446170dup
GRCh38.p14 chr 11	NC_000011.10:g.126446167_126446170dup
GRCh38.p14 chr 11	NC_000011.10:g.126446166_126446170dup
GRCh38.p14 chr 11	NC_000011.10:g.126446165_126446170dup
GRCh38.p14 chr 11	NC_000011.10:g.126446161_126446170dup
GRCh38.p14 chr 11	NC_000011.10:g.126446153_126446170dup
GRCh38.p14 chr 11	NC_000011.10:g.126446149_126446170dup
GRCh37.p13 chr 11	NC_000011.9:g.126316058_126316065del
GRCh37.p13 chr 11	NC_000011.9:g.126316059_126316065del
GRCh37.p13 chr 11	NC_000011.9:g.126316062_126316065del
GRCh37.p13 chr 11	NC_000011.9:g.126316063_126316065del
GRCh37.p13 chr 11	NC_000011.9:g.126316064_126316065del
GRCh37.p13 chr 11	NC_000011.9:g.126316065del
GRCh37.p13 chr 11	NC_000011.9:g.126316065dup
GRCh37.p13 chr 11	NC_000011.9:g.126316064_126316065dup
GRCh37.p13 chr 11	NC_000011.9:g.126316063_126316065dup
GRCh37.p13 chr 11	NC_000011.9:g.126316062_126316065dup
GRCh37.p13 chr 11	NC_000011.9:g.126316061_126316065dup
GRCh37.p13 chr 11	NC_000011.9:g.126316060_126316065dup
GRCh37.p13 chr 11	NC_000011.9:g.126316056_126316065dup
GRCh37.p13 chr 11	NC_000011.9:g.126316048_126316065dup
GRCh37.p13 chr 11	NC_000011.9:g.126316044_126316065dup
KIRREL3 RefSeqGene	NG_012971.2:g.559714_559721del
KIRREL3 RefSeqGene	NG_012971.2:g.559715_559721del
KIRREL3 RefSeqGene	NG_012971.2:g.559718_559721del
KIRREL3 RefSeqGene	NG_012971.2:g.559719_559721del
KIRREL3 RefSeqGene	NG_012971.2:g.559720_559721del
KIRREL3 RefSeqGene	NG_012971.2:g.559721del
KIRREL3 RefSeqGene	NG_012971.2:g.559721dup
KIRREL3 RefSeqGene	NG_012971.2:g.559720_559721dup
KIRREL3 RefSeqGene	NG_012971.2:g.559719_559721dup
KIRREL3 RefSeqGene	NG_012971.2:g.559718_559721dup
KIRREL3 RefSeqGene	NG_012971.2:g.559717_559721dup
KIRREL3 RefSeqGene	NG_012971.2:g.559716_559721dup
KIRREL3 RefSeqGene	NG_012971.2:g.559712_559721dup
KIRREL3 RefSeqGene	NG_012971.2:g.559704_559721dup
KIRREL3 RefSeqGene	NG_012971.2:g.559700_559721dup
KIRREL3 RefSeqGene	NG_012971.1:g.559716_559723del
KIRREL3 RefSeqGene	NG_012971.1:g.559717_559723del
KIRREL3 RefSeqGene	NG_012971.1:g.559720_559723del
KIRREL3 RefSeqGene	NG_012971.1:g.559721_559723del
KIRREL3 RefSeqGene	NG_012971.1:g.559722_559723del
KIRREL3 RefSeqGene	NG_012971.1:g.559723del
KIRREL3 RefSeqGene	NG_012971.1:g.559723dup
KIRREL3 RefSeqGene	NG_012971.1:g.559722_559723dup
KIRREL3 RefSeqGene	NG_012971.1:g.559721_559723dup
KIRREL3 RefSeqGene	NG_012971.1:g.559720_559723dup
KIRREL3 RefSeqGene	NG_012971.1:g.559719_559723dup
KIRREL3 RefSeqGene	NG_012971.1:g.559718_559723dup
KIRREL3 RefSeqGene	NG_012971.1:g.559714_559723dup
KIRREL3 RefSeqGene	NG_012971.1:g.559706_559723dup
KIRREL3 RefSeqGene	NG_012971.1:g.559702_559723dup
ST3GAL4 RefSeqGene	NG_053025.1:g.95519_95526del
ST3GAL4 RefSeqGene	NG_053025.1:g.95520_95526del
ST3GAL4 RefSeqGene	NG_053025.1:g.95523_95526del
ST3GAL4 RefSeqGene	NG_053025.1:g.95524_95526del
ST3GAL4 RefSeqGene	NG_053025.1:g.95525_95526del
ST3GAL4 RefSeqGene	NG_053025.1:g.95526del
ST3GAL4 RefSeqGene	NG_053025.1:g.95526dup
ST3GAL4 RefSeqGene	NG_053025.1:g.95525_95526dup
ST3GAL4 RefSeqGene	NG_053025.1:g.95524_95526dup
ST3GAL4 RefSeqGene	NG_053025.1:g.95523_95526dup
ST3GAL4 RefSeqGene	NG_053025.1:g.95522_95526dup
ST3GAL4 RefSeqGene	NG_053025.1:g.95521_95526dup
ST3GAL4 RefSeqGene	NG_053025.1:g.95517_95526dup
ST3GAL4 RefSeqGene	NG_053025.1:g.95509_95526dup
ST3GAL4 RefSeqGene	NG_053025.1:g.95505_95526dup

Gene: KIRREL3, kirre like nephrin family adhesion molecule 3 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
KIRREL3 transcript variant 2	NM_001161707.1:c.1125+603… NM_001161707.1:c.1125+603_1125+610del	N/A	Intron Variant
KIRREL3 transcript variant 3	NM_001301097.1:c.1125+603… NM_001301097.1:c.1125+603_1125+610del	N/A	Intron Variant
KIRREL3 transcript variant 1	NM_032531.4:c.1125+603_11… NM_032531.4:c.1125+603_1125+610del	N/A	Intron Variant
KIRREL3 transcript variant X1	XM_011543026.3:c.1143+603… XM_011543026.3:c.1143+603_1143+610del	N/A	Intron Variant
KIRREL3 transcript variant X5	XM_011543027.3:c.1125+603… XM_011543027.3:c.1125+603_1125+610del	N/A	Intron Variant
KIRREL3 transcript variant X2	XM_011543030.4:c.1143+603… XM_011543030.4:c.1143+603_1143+610del	N/A	Intron Variant
KIRREL3 transcript variant X3	XM_011543032.4:c.1143+603… XM_011543032.4:c.1143+603_1143+610del	N/A	Intron Variant
KIRREL3 transcript variant X6	XM_017018419.2:c.1125+603… XM_017018419.2:c.1125+603_1125+610del	N/A	Intron Variant
KIRREL3 transcript variant X4	XM_047427715.1:c.558+603_… XM_047427715.1:c.558+603_558+610del	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	(A)₂₂=	del(A)₈	del(A)₇	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₁₀	dup(A)₁₈	dup(A)₂₂
GRCh38.p14 chr 11	NC_000011.10:g.126446149_126446170=	NC_000011.10:g.126446163_126446170del	NC_000011.10:g.126446164_126446170del	NC_000011.10:g.126446167_126446170del	NC_000011.10:g.126446168_126446170del	NC_000011.10:g.126446169_126446170del	NC_000011.10:g.126446170del	NC_000011.10:g.126446170dup	NC_000011.10:g.126446169_126446170dup	NC_000011.10:g.126446168_126446170dup	NC_000011.10:g.126446167_126446170dup	NC_000011.10:g.126446166_126446170dup	NC_000011.10:g.126446165_126446170dup	NC_000011.10:g.126446161_126446170dup	NC_000011.10:g.126446153_126446170dup	NC_000011.10:g.126446149_126446170dup
GRCh37.p13 chr 11	NC_000011.9:g.126316044_126316065=	NC_000011.9:g.126316058_126316065del	NC_000011.9:g.126316059_126316065del	NC_000011.9:g.126316062_126316065del	NC_000011.9:g.126316063_126316065del	NC_000011.9:g.126316064_126316065del	NC_000011.9:g.126316065del	NC_000011.9:g.126316065dup	NC_000011.9:g.126316064_126316065dup	NC_000011.9:g.126316063_126316065dup	NC_000011.9:g.126316062_126316065dup	NC_000011.9:g.126316061_126316065dup	NC_000011.9:g.126316060_126316065dup	NC_000011.9:g.126316056_126316065dup	NC_000011.9:g.126316048_126316065dup	NC_000011.9:g.126316044_126316065dup
KIRREL3 RefSeqGene	NG_012971.2:g.559700_559721=	NG_012971.2:g.559714_559721del	NG_012971.2:g.559715_559721del	NG_012971.2:g.559718_559721del	NG_012971.2:g.559719_559721del	NG_012971.2:g.559720_559721del	NG_012971.2:g.559721del	NG_012971.2:g.559721dup	NG_012971.2:g.559720_559721dup	NG_012971.2:g.559719_559721dup	NG_012971.2:g.559718_559721dup	NG_012971.2:g.559717_559721dup	NG_012971.2:g.559716_559721dup	NG_012971.2:g.559712_559721dup	NG_012971.2:g.559704_559721dup	NG_012971.2:g.559700_559721dup
KIRREL3 RefSeqGene	NG_012971.1:g.559702_559723=	NG_012971.1:g.559716_559723del	NG_012971.1:g.559717_559723del	NG_012971.1:g.559720_559723del	NG_012971.1:g.559721_559723del	NG_012971.1:g.559722_559723del	NG_012971.1:g.559723del	NG_012971.1:g.559723dup	NG_012971.1:g.559722_559723dup	NG_012971.1:g.559721_559723dup	NG_012971.1:g.559720_559723dup	NG_012971.1:g.559719_559723dup	NG_012971.1:g.559718_559723dup	NG_012971.1:g.559714_559723dup	NG_012971.1:g.559706_559723dup	NG_012971.1:g.559702_559723dup
ST3GAL4 RefSeqGene	NG_053025.1:g.95505_95526=	NG_053025.1:g.95519_95526del	NG_053025.1:g.95520_95526del	NG_053025.1:g.95523_95526del	NG_053025.1:g.95524_95526del	NG_053025.1:g.95525_95526del	NG_053025.1:g.95526del	NG_053025.1:g.95526dup	NG_053025.1:g.95525_95526dup	NG_053025.1:g.95524_95526dup	NG_053025.1:g.95523_95526dup	NG_053025.1:g.95522_95526dup	NG_053025.1:g.95521_95526dup	NG_053025.1:g.95517_95526dup	NG_053025.1:g.95509_95526dup	NG_053025.1:g.95505_95526dup
KIRREL3 transcript variant 2	NM_001161707.1:c.1125+610=	NM_001161707.1:c.1125+603_1125+610del	NM_001161707.1:c.1125+604_1125+610del	NM_001161707.1:c.1125+607_1125+610del	NM_001161707.1:c.1125+608_1125+610del	NM_001161707.1:c.1125+609_1125+610del	NM_001161707.1:c.1125+610del	NM_001161707.1:c.1125+610dup	NM_001161707.1:c.1125+609_1125+610dup	NM_001161707.1:c.1125+608_1125+610dup	NM_001161707.1:c.1125+607_1125+610dup	NM_001161707.1:c.1125+606_1125+610dup	NM_001161707.1:c.1125+605_1125+610dup	NM_001161707.1:c.1125+601_1125+610dup	NM_001161707.1:c.1125+593_1125+610dup	NM_001161707.1:c.1125+589_1125+610dup
KIRREL3 transcript variant 3	NM_001301097.1:c.1125+610=	NM_001301097.1:c.1125+603_1125+610del	NM_001301097.1:c.1125+604_1125+610del	NM_001301097.1:c.1125+607_1125+610del	NM_001301097.1:c.1125+608_1125+610del	NM_001301097.1:c.1125+609_1125+610del	NM_001301097.1:c.1125+610del	NM_001301097.1:c.1125+610dup	NM_001301097.1:c.1125+609_1125+610dup	NM_001301097.1:c.1125+608_1125+610dup	NM_001301097.1:c.1125+607_1125+610dup	NM_001301097.1:c.1125+606_1125+610dup	NM_001301097.1:c.1125+605_1125+610dup	NM_001301097.1:c.1125+601_1125+610dup	NM_001301097.1:c.1125+593_1125+610dup	NM_001301097.1:c.1125+589_1125+610dup
KIRREL3 transcript variant 1	NM_032531.3:c.1125+610=	NM_032531.3:c.1125+603_1125+610del	NM_032531.3:c.1125+604_1125+610del	NM_032531.3:c.1125+607_1125+610del	NM_032531.3:c.1125+608_1125+610del	NM_032531.3:c.1125+609_1125+610del	NM_032531.3:c.1125+610del	NM_032531.3:c.1125+610dup	NM_032531.3:c.1125+609_1125+610dup	NM_032531.3:c.1125+608_1125+610dup	NM_032531.3:c.1125+607_1125+610dup	NM_032531.3:c.1125+606_1125+610dup	NM_032531.3:c.1125+605_1125+610dup	NM_032531.3:c.1125+601_1125+610dup	NM_032531.3:c.1125+593_1125+610dup	NM_032531.3:c.1125+589_1125+610dup
KIRREL3 transcript variant 1	NM_032531.4:c.1125+610=	NM_032531.4:c.1125+603_1125+610del	NM_032531.4:c.1125+604_1125+610del	NM_032531.4:c.1125+607_1125+610del	NM_032531.4:c.1125+608_1125+610del	NM_032531.4:c.1125+609_1125+610del	NM_032531.4:c.1125+610del	NM_032531.4:c.1125+610dup	NM_032531.4:c.1125+609_1125+610dup	NM_032531.4:c.1125+608_1125+610dup	NM_032531.4:c.1125+607_1125+610dup	NM_032531.4:c.1125+606_1125+610dup	NM_032531.4:c.1125+605_1125+610dup	NM_032531.4:c.1125+601_1125+610dup	NM_032531.4:c.1125+593_1125+610dup	NM_032531.4:c.1125+589_1125+610dup
KIRREL3 transcript variant X1	XM_005271702.1:c.1125+610=	XM_005271702.1:c.1125+603_1125+610del	XM_005271702.1:c.1125+604_1125+610del	XM_005271702.1:c.1125+607_1125+610del	XM_005271702.1:c.1125+608_1125+610del	XM_005271702.1:c.1125+609_1125+610del	XM_005271702.1:c.1125+610del	XM_005271702.1:c.1125+610dup	XM_005271702.1:c.1125+609_1125+610dup	XM_005271702.1:c.1125+608_1125+610dup	XM_005271702.1:c.1125+607_1125+610dup	XM_005271702.1:c.1125+606_1125+610dup	XM_005271702.1:c.1125+605_1125+610dup	XM_005271702.1:c.1125+601_1125+610dup	XM_005271702.1:c.1125+593_1125+610dup	XM_005271702.1:c.1125+589_1125+610dup
KIRREL3 transcript variant X1	XM_011543026.3:c.1143+610=	XM_011543026.3:c.1143+603_1143+610del	XM_011543026.3:c.1143+604_1143+610del	XM_011543026.3:c.1143+607_1143+610del	XM_011543026.3:c.1143+608_1143+610del	XM_011543026.3:c.1143+609_1143+610del	XM_011543026.3:c.1143+610del	XM_011543026.3:c.1143+610dup	XM_011543026.3:c.1143+609_1143+610dup	XM_011543026.3:c.1143+608_1143+610dup	XM_011543026.3:c.1143+607_1143+610dup	XM_011543026.3:c.1143+606_1143+610dup	XM_011543026.3:c.1143+605_1143+610dup	XM_011543026.3:c.1143+601_1143+610dup	XM_011543026.3:c.1143+593_1143+610dup	XM_011543026.3:c.1143+589_1143+610dup
KIRREL3 transcript variant X5	XM_011543027.3:c.1125+610=	XM_011543027.3:c.1125+603_1125+610del	XM_011543027.3:c.1125+604_1125+610del	XM_011543027.3:c.1125+607_1125+610del	XM_011543027.3:c.1125+608_1125+610del	XM_011543027.3:c.1125+609_1125+610del	XM_011543027.3:c.1125+610del	XM_011543027.3:c.1125+610dup	XM_011543027.3:c.1125+609_1125+610dup	XM_011543027.3:c.1125+608_1125+610dup	XM_011543027.3:c.1125+607_1125+610dup	XM_011543027.3:c.1125+606_1125+610dup	XM_011543027.3:c.1125+605_1125+610dup	XM_011543027.3:c.1125+601_1125+610dup	XM_011543027.3:c.1125+593_1125+610dup	XM_011543027.3:c.1125+589_1125+610dup
KIRREL3 transcript variant X2	XM_011543030.4:c.1143+610=	XM_011543030.4:c.1143+603_1143+610del	XM_011543030.4:c.1143+604_1143+610del	XM_011543030.4:c.1143+607_1143+610del	XM_011543030.4:c.1143+608_1143+610del	XM_011543030.4:c.1143+609_1143+610del	XM_011543030.4:c.1143+610del	XM_011543030.4:c.1143+610dup	XM_011543030.4:c.1143+609_1143+610dup	XM_011543030.4:c.1143+608_1143+610dup	XM_011543030.4:c.1143+607_1143+610dup	XM_011543030.4:c.1143+606_1143+610dup	XM_011543030.4:c.1143+605_1143+610dup	XM_011543030.4:c.1143+601_1143+610dup	XM_011543030.4:c.1143+593_1143+610dup	XM_011543030.4:c.1143+589_1143+610dup
KIRREL3 transcript variant X3	XM_011543032.4:c.1143+610=	XM_011543032.4:c.1143+603_1143+610del	XM_011543032.4:c.1143+604_1143+610del	XM_011543032.4:c.1143+607_1143+610del	XM_011543032.4:c.1143+608_1143+610del	XM_011543032.4:c.1143+609_1143+610del	XM_011543032.4:c.1143+610del	XM_011543032.4:c.1143+610dup	XM_011543032.4:c.1143+609_1143+610dup	XM_011543032.4:c.1143+608_1143+610dup	XM_011543032.4:c.1143+607_1143+610dup	XM_011543032.4:c.1143+606_1143+610dup	XM_011543032.4:c.1143+605_1143+610dup	XM_011543032.4:c.1143+601_1143+610dup	XM_011543032.4:c.1143+593_1143+610dup	XM_011543032.4:c.1143+589_1143+610dup
KIRREL3 transcript variant X6	XM_017018419.2:c.1125+610=	XM_017018419.2:c.1125+603_1125+610del	XM_017018419.2:c.1125+604_1125+610del	XM_017018419.2:c.1125+607_1125+610del	XM_017018419.2:c.1125+608_1125+610del	XM_017018419.2:c.1125+609_1125+610del	XM_017018419.2:c.1125+610del	XM_017018419.2:c.1125+610dup	XM_017018419.2:c.1125+609_1125+610dup	XM_017018419.2:c.1125+608_1125+610dup	XM_017018419.2:c.1125+607_1125+610dup	XM_017018419.2:c.1125+606_1125+610dup	XM_017018419.2:c.1125+605_1125+610dup	XM_017018419.2:c.1125+601_1125+610dup	XM_017018419.2:c.1125+593_1125+610dup	XM_017018419.2:c.1125+589_1125+610dup
KIRREL3 transcript variant X4	XM_047427715.1:c.558+610=	XM_047427715.1:c.558+603_558+610del	XM_047427715.1:c.558+604_558+610del	XM_047427715.1:c.558+607_558+610del	XM_047427715.1:c.558+608_558+610del	XM_047427715.1:c.558+609_558+610del	XM_047427715.1:c.558+610del	XM_047427715.1:c.558+610dup	XM_047427715.1:c.558+609_558+610dup	XM_047427715.1:c.558+608_558+610dup	XM_047427715.1:c.558+607_558+610dup	XM_047427715.1:c.558+606_558+610dup	XM_047427715.1:c.558+605_558+610dup	XM_047427715.1:c.558+601_558+610dup	XM_047427715.1:c.558+593_558+610dup	XM_047427715.1:c.558+589_558+610dup

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#.

55 SubSNP, 29 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80405749	Dec 14, 2007 (129)
2	PJP	ss294728636	May 09, 2011 (134)
3	EVA_GENOME_DK	ss1574431514	Apr 01, 2015 (144)
4	EVA_UK10K_ALSPAC	ss1707300381	Apr 01, 2015 (144)
5	EVA_UK10K_TWINSUK	ss1707300519	Apr 01, 2015 (144)
6	EVA_UK10K_ALSPAC	ss1710538205	Apr 01, 2015 (144)
7	EVA_UK10K_TWINSUK	ss1710538210	Apr 01, 2015 (144)
8	SWEGEN	ss3008955725	Nov 08, 2017 (151)
9	MCHAISSO	ss3065454782	Nov 08, 2017 (151)
10	EVA_DECODE	ss3692814005	Jul 13, 2019 (153)
11	EVA_DECODE	ss3692814006	Jul 13, 2019 (153)
12	EVA_DECODE	ss3692814007	Jul 13, 2019 (153)
13	EVA_DECODE	ss3692814008	Jul 13, 2019 (153)
14	EVA_DECODE	ss3692814009	Jul 13, 2019 (153)
15	PACBIO	ss3792217572	Jul 13, 2019 (153)
16	PACBIO	ss3792217573	Jul 13, 2019 (153)
17	PACBIO	ss3797100101	Jul 13, 2019 (153)
18	PACBIO	ss3797100102	Jul 13, 2019 (153)
19	EVA	ss3832894474	Apr 26, 2020 (154)
20	GNOMAD	ss4244445649	Apr 26, 2021 (155)
21	GNOMAD	ss4244445650	Apr 26, 2021 (155)
22	GNOMAD	ss4244445651	Apr 26, 2021 (155)
23	GNOMAD	ss4244445652	Apr 26, 2021 (155)
24	GNOMAD	ss4244445653	Apr 26, 2021 (155)
25	GNOMAD	ss4244445654	Apr 26, 2021 (155)
26	GNOMAD	ss4244445655	Apr 26, 2021 (155)
27	GNOMAD	ss4244445656	Apr 26, 2021 (155)
28	GNOMAD	ss4244445657	Apr 26, 2021 (155)
29	GNOMAD	ss4244445658	Apr 26, 2021 (155)
30	GNOMAD	ss4244445659	Apr 26, 2021 (155)
31	GNOMAD	ss4244445660	Apr 26, 2021 (155)
32	GNOMAD	ss4244445661	Apr 26, 2021 (155)
33	GNOMAD	ss4244445662	Apr 26, 2021 (155)
34	GNOMAD	ss4244445663	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5204380184	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5204380185	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5204380186	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5204380187	Apr 26, 2021 (155)
39	1000G_HIGH_COVERAGE	ss5289279456	Oct 16, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5289279457	Oct 16, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5289279459	Oct 16, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5289279460	Oct 16, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5289279461	Oct 16, 2022 (156)
44	HUGCELL_USP	ss5484230184	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5484230185	Oct 16, 2022 (156)
46	HUGCELL_USP	ss5484230186	Oct 16, 2022 (156)
47	HUGCELL_USP	ss5484230187	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5752972096	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5752972097	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5752972098	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5752972100	Oct 16, 2022 (156)
52	EVA	ss5837378807	Oct 16, 2022 (156)
53	EVA	ss5837378808	Oct 16, 2022 (156)
54	EVA	ss5837378809	Oct 16, 2022 (156)
55	EVA	ss5837378810	Oct 16, 2022 (156)
56	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 31092700 (NC_000011.9:126316043::AA 1797/3854) Row 31092701 (NC_000011.9:126316043:AA: 1560/3854)	-	Oct 12, 2018 (152)
57	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 31092700 (NC_000011.9:126316043::AA 1797/3854) Row 31092701 (NC_000011.9:126316043:AA: 1560/3854)	-	Oct 12, 2018 (152)
58	The Danish reference pan genome	NC_000011.9 - 126316044	Apr 26, 2020 (154)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 395054962 (NC_000011.10:126446148::A 3363/76296) Row 395054963 (NC_000011.10:126446148::AA 12846/76158) Row 395054964 (NC_000011.10:126446148::AAA 1182/76176)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 395054962 (NC_000011.10:126446148::A 3363/76296) Row 395054963 (NC_000011.10:126446148::AA 12846/76158) Row 395054964 (NC_000011.10:126446148::AAA 1182/76176)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 395054962 (NC_000011.10:126446148::A 3363/76296) Row 395054963 (NC_000011.10:126446148::AA 12846/76158) Row 395054964 (NC_000011.10:126446148::AAA 1182/76176)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 395054962 (NC_000011.10:126446148::A 3363/76296) Row 395054963 (NC_000011.10:126446148::AA 12846/76158) Row 395054964 (NC_000011.10:126446148::AAA 1182/76176)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 395054962 (NC_000011.10:126446148::A 3363/76296) Row 395054963 (NC_000011.10:126446148::AA 12846/76158) Row 395054964 (NC_000011.10:126446148::AAA 1182/76176)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 395054962 (NC_000011.10:126446148::A 3363/76296) Row 395054963 (NC_000011.10:126446148::AA 12846/76158) Row 395054964 (NC_000011.10:126446148::AAA 1182/76176)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 395054962 (NC_000011.10:126446148::A 3363/76296) Row 395054963 (NC_000011.10:126446148::AA 12846/76158) Row 395054964 (NC_000011.10:126446148::AAA 1182/76176)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 395054962 (NC_000011.10:126446148::A 3363/76296) Row 395054963 (NC_000011.10:126446148::AA 12846/76158) Row 395054964 (NC_000011.10:126446148::AAA 1182/76176)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 395054962 (NC_000011.10:126446148::A 3363/76296) Row 395054963 (NC_000011.10:126446148::AA 12846/76158) Row 395054964 (NC_000011.10:126446148::AAA 1182/76176)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 395054962 (NC_000011.10:126446148::A 3363/76296) Row 395054963 (NC_000011.10:126446148::AA 12846/76158) Row 395054964 (NC_000011.10:126446148::AAA 1182/76176)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 395054962 (NC_000011.10:126446148::A 3363/76296) Row 395054963 (NC_000011.10:126446148::AA 12846/76158) Row 395054964 (NC_000011.10:126446148::AAA 1182/76176)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 395054962 (NC_000011.10:126446148::A 3363/76296) Row 395054963 (NC_000011.10:126446148::AA 12846/76158) Row 395054964 (NC_000011.10:126446148::AAA 1182/76176)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 395054962 (NC_000011.10:126446148::A 3363/76296) Row 395054963 (NC_000011.10:126446148::AA 12846/76158) Row 395054964 (NC_000011.10:126446148::AAA 1182/76176)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 395054962 (NC_000011.10:126446148::A 3363/76296) Row 395054963 (NC_000011.10:126446148::AA 12846/76158) Row 395054964 (NC_000011.10:126446148::AAA 1182/76176)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 395054962 (NC_000011.10:126446148::A 3363/76296) Row 395054963 (NC_000011.10:126446148::AA 12846/76158) Row 395054964 (NC_000011.10:126446148::AAA 1182/76176)...	-	Apr 26, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 62349491 (NC_000011.9:126316043:A: 4513/16030) Row 62349492 (NC_000011.9:126316043::A 3779/16030) Row 62349493 (NC_000011.9:126316043:AA: 48/16030)...	-	Apr 26, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 62349491 (NC_000011.9:126316043:A: 4513/16030) Row 62349492 (NC_000011.9:126316043::A 3779/16030) Row 62349493 (NC_000011.9:126316043:AA: 48/16030)...	-	Apr 26, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 62349491 (NC_000011.9:126316043:A: 4513/16030) Row 62349492 (NC_000011.9:126316043::A 3779/16030) Row 62349493 (NC_000011.9:126316043:AA: 48/16030)...	-	Apr 26, 2021 (155)
77	8.3KJPN Submission ignored due to conflicting rows: Row 62349491 (NC_000011.9:126316043:A: 4513/16030) Row 62349492 (NC_000011.9:126316043::A 3779/16030) Row 62349493 (NC_000011.9:126316043:AA: 48/16030)...	-	Apr 26, 2021 (155)
78	14KJPN Submission ignored due to conflicting rows: Row 86809200 (NC_000011.10:126446148:A: 8379/27842) Row 86809201 (NC_000011.10:126446148::A 6713/27842) Row 86809202 (NC_000011.10:126446148:AA: 87/27842)...	-	Oct 16, 2022 (156)
79	14KJPN Submission ignored due to conflicting rows: Row 86809200 (NC_000011.10:126446148:A: 8379/27842) Row 86809201 (NC_000011.10:126446148::A 6713/27842) Row 86809202 (NC_000011.10:126446148:AA: 87/27842)...	-	Oct 16, 2022 (156)
80	14KJPN Submission ignored due to conflicting rows: Row 86809200 (NC_000011.10:126446148:A: 8379/27842) Row 86809201 (NC_000011.10:126446148::A 6713/27842) Row 86809202 (NC_000011.10:126446148:AA: 87/27842)...	-	Oct 16, 2022 (156)
81	14KJPN Submission ignored due to conflicting rows: Row 86809200 (NC_000011.10:126446148:A: 8379/27842) Row 86809201 (NC_000011.10:126446148::A 6713/27842) Row 86809202 (NC_000011.10:126446148:AA: 87/27842)...	-	Oct 16, 2022 (156)
82	UK 10K study - Twins Submission ignored due to conflicting rows: Row 31092700 (NC_000011.9:126316043::AA 1608/3708) Row 31092701 (NC_000011.9:126316043:AA: 1574/3708)	-	Oct 12, 2018 (152)
83	UK 10K study - Twins Submission ignored due to conflicting rows: Row 31092700 (NC_000011.9:126316043::AA 1608/3708) Row 31092701 (NC_000011.9:126316043:AA: 1574/3708)	-	Oct 12, 2018 (152)
84	ALFA	NC_000011.10 - 126446149	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)
rs66522025	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4244445663	NC_000011.10:126446148:AAAAAAAA:	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
5768272082	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4244445662	NC_000011.10:126446148:AAAAAAA:	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
5768272082	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4244445661	NC_000011.10:126446148:AAAA:	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
5768272082	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3692814009, ss4244445660	NC_000011.10:126446148:AAA:	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
5768272082	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss1707300381, ss1707300519, ss3008955725, ss3832894474, ss5204380186, ss5837378809	NC_000011.9:126316043:AA:	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3065454782, ss4244445659, ss5289279461, ss5484230184, ss5752972098	NC_000011.10:126446148:AA:	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
5768272082	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3692814008	NC_000011.10:126446149:AA:	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss80405749, ss294728636	NC_000011.8:125821274:A:	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
327523, ss1574431514, ss5204380184, ss5837378808	NC_000011.9:126316043:A:	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4244445658, ss5289279456, ss5484230185, ss5752972096	NC_000011.10:126446148:A:	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
5768272082	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3692814007	NC_000011.10:126446150:A:	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3792217572, ss3797100101, ss5204380185	NC_000011.9:126316043::A	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4244445649, ss5289279460, ss5484230187, ss5752972097	NC_000011.10:126446148::A	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
5768272082	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3692814006	NC_000011.10:126446151::A	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3792217573, ss3797100102, ss5204380187, ss5837378807	NC_000011.9:126316043::AA	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss1710538205, ss1710538210	NC_000011.9:126316045::AA	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4244445650, ss5289279457, ss5484230186, ss5752972100	NC_000011.10:126446148::AA	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
5768272082	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3692814005	NC_000011.10:126446151::AA	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5837378810	NC_000011.9:126316043::AAA	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA
ss4244445651, ss5289279459	NC_000011.10:126446148::AAA	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
5768272082	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4244445652	NC_000011.10:126446148::AAAA	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
5768272082	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4244445653	NC_000011.10:126446148::AAAAA	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
5768272082	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4244445654	NC_000011.10:126446148::AAAAAA	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4244445655	NC_000011.10:126446148::AAAAAAAAAA	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4244445656	NC_000011.10:126446148::AAAAAAAAAA… NC_000011.10:126446148::AAAAAAAAAAAAAAAAAA	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4244445657	NC_000011.10:126446148::AAAAAAAAAA… NC_000011.10:126446148::AAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:126446148:AAAAAAAAAAA… NC_000011.10:126446148:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

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

No publications for rs56820180

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
Top▲ Help
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.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs56820180