Name: rs766173367
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.

rs766173367

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:10885889-10885914 (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(T)₁₃ / del(T)₁₂ / del(T)₁₀ / d…
del(T)₁₃ / del(T)₁₂ / del(T)₁₀ / del(T)₉ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₃=0.00000 (0/13540, ALFA)
del(T)₁₂=0.00000 (0/13540, ALFA)
del(T)₁₀=0.00000 (0/13540, ALFA) (+ 9 more)
del(T)₉=0.00000 (0/13540, ALFA)
del(T)₈=0.00000 (0/13540, ALFA)
del(T)₇=0.00000 (0/13540, ALFA)
del(T)₆=0.00000 (0/13540, ALFA)
del(T)₄=0.00000 (0/13540, ALFA)
delTTT=0.00000 (0/13540, ALFA)
delTT=0.00000 (0/13540, ALFA)
delT=0.00000 (0/13540, ALFA)
dupT=0.00000 (0/13540, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CARM1 : 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	13540	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.00000	TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	1.0	N/A
European	Sub	9602	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	2692	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	100	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	2592	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	64	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	50	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	14	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	134	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
Latin American 2	Sub	498	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	96	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	454	TTTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	13540	(T)₂₆=1.00000	del(T)₁₃=0.00000, del(T)₁₂=0.00000, del(T)₁₀=0.00000, del(T)₉=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00000, dupT=0.00000
Allele Frequency Aggregator	European	Sub	9602	(T)₂₆=1.0000	del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000
Allele Frequency Aggregator	African	Sub	2692	(T)₂₆=1.0000	del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	498	(T)₂₆=1.000	del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000
Allele Frequency Aggregator	Other	Sub	454	(T)₂₆=1.000	del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	134	(T)₂₆=1.000	del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000
Allele Frequency Aggregator	South Asian	Sub	96	(T)₂₆=1.00	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00
Allele Frequency Aggregator	Asian	Sub	64	(T)₂₆=1.00	del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00

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 19	NC_000019.10:g.10885902_10885914del
GRCh38.p14 chr 19	NC_000019.10:g.10885903_10885914del
GRCh38.p14 chr 19	NC_000019.10:g.10885905_10885914del
GRCh38.p14 chr 19	NC_000019.10:g.10885906_10885914del
GRCh38.p14 chr 19	NC_000019.10:g.10885907_10885914del
GRCh38.p14 chr 19	NC_000019.10:g.10885908_10885914del
GRCh38.p14 chr 19	NC_000019.10:g.10885909_10885914del
GRCh38.p14 chr 19	NC_000019.10:g.10885910_10885914del
GRCh38.p14 chr 19	NC_000019.10:g.10885911_10885914del
GRCh38.p14 chr 19	NC_000019.10:g.10885912_10885914del
GRCh38.p14 chr 19	NC_000019.10:g.10885913_10885914del
GRCh38.p14 chr 19	NC_000019.10:g.10885914del
GRCh38.p14 chr 19	NC_000019.10:g.10885914dup
GRCh38.p14 chr 19	NC_000019.10:g.10885913_10885914dup
GRCh38.p14 chr 19	NC_000019.10:g.10885912_10885914dup
GRCh37.p13 chr 19	NC_000019.9:g.10996578_10996590del
GRCh37.p13 chr 19	NC_000019.9:g.10996579_10996590del
GRCh37.p13 chr 19	NC_000019.9:g.10996581_10996590del
GRCh37.p13 chr 19	NC_000019.9:g.10996582_10996590del
GRCh37.p13 chr 19	NC_000019.9:g.10996583_10996590del
GRCh37.p13 chr 19	NC_000019.9:g.10996584_10996590del
GRCh37.p13 chr 19	NC_000019.9:g.10996585_10996590del
GRCh37.p13 chr 19	NC_000019.9:g.10996586_10996590del
GRCh37.p13 chr 19	NC_000019.9:g.10996587_10996590del
GRCh37.p13 chr 19	NC_000019.9:g.10996588_10996590del
GRCh37.p13 chr 19	NC_000019.9:g.10996589_10996590del
GRCh37.p13 chr 19	NC_000019.9:g.10996590del
GRCh37.p13 chr 19	NC_000019.9:g.10996590dup
GRCh37.p13 chr 19	NC_000019.9:g.10996589_10996590dup
GRCh37.p13 chr 19	NC_000019.9:g.10996588_10996590dup

Gene: CARM1, coactivator associated arginine methyltransferase 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CARM1 transcript variant 2	NM_001370088.1:c.220+1398… NM_001370088.1:c.220+13980_220+13992del	N/A	Intron Variant
CARM1 transcript variant 3	NM_001370089.1:c.115+1331… NM_001370089.1:c.115+13310_115+13322del	N/A	Intron Variant
CARM1 transcript variant 1	NM_199141.2:c.220+13980_2… NM_199141.2:c.220+13980_220+13992del	N/A	Intron Variant
CARM1 transcript variant X1	XM_047438058.1:c.115+1331… XM_047438058.1:c.115+13310_115+13322del	N/A	Intron Variant
CARM1 transcript variant X2	XM_011527638.3:c.	N/A	Genic Upstream Transcript 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	(T)₂₆=	del(T)₁₃	del(T)₁₂	del(T)₁₀	del(T)₉	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT
GRCh38.p14 chr 19	NC_000019.10:g.10885889_10885914=	NC_000019.10:g.10885902_10885914del	NC_000019.10:g.10885903_10885914del	NC_000019.10:g.10885905_10885914del	NC_000019.10:g.10885906_10885914del	NC_000019.10:g.10885907_10885914del	NC_000019.10:g.10885908_10885914del	NC_000019.10:g.10885909_10885914del	NC_000019.10:g.10885910_10885914del	NC_000019.10:g.10885911_10885914del	NC_000019.10:g.10885912_10885914del	NC_000019.10:g.10885913_10885914del	NC_000019.10:g.10885914del	NC_000019.10:g.10885914dup	NC_000019.10:g.10885913_10885914dup	NC_000019.10:g.10885912_10885914dup
GRCh37.p13 chr 19	NC_000019.9:g.10996565_10996590=	NC_000019.9:g.10996578_10996590del	NC_000019.9:g.10996579_10996590del	NC_000019.9:g.10996581_10996590del	NC_000019.9:g.10996582_10996590del	NC_000019.9:g.10996583_10996590del	NC_000019.9:g.10996584_10996590del	NC_000019.9:g.10996585_10996590del	NC_000019.9:g.10996586_10996590del	NC_000019.9:g.10996587_10996590del	NC_000019.9:g.10996588_10996590del	NC_000019.9:g.10996589_10996590del	NC_000019.9:g.10996590del	NC_000019.9:g.10996590dup	NC_000019.9:g.10996589_10996590dup	NC_000019.9:g.10996588_10996590dup
CARM1 transcript variant 2	NM_001370088.1:c.220+13967=	NM_001370088.1:c.220+13980_220+13992del	NM_001370088.1:c.220+13981_220+13992del	NM_001370088.1:c.220+13983_220+13992del	NM_001370088.1:c.220+13984_220+13992del	NM_001370088.1:c.220+13985_220+13992del	NM_001370088.1:c.220+13986_220+13992del	NM_001370088.1:c.220+13987_220+13992del	NM_001370088.1:c.220+13988_220+13992del	NM_001370088.1:c.220+13989_220+13992del	NM_001370088.1:c.220+13990_220+13992del	NM_001370088.1:c.220+13991_220+13992del	NM_001370088.1:c.220+13992del	NM_001370088.1:c.220+13992dup	NM_001370088.1:c.220+13991_220+13992dup	NM_001370088.1:c.220+13990_220+13992dup
CARM1 transcript variant 3	NM_001370089.1:c.115+13297=	NM_001370089.1:c.115+13310_115+13322del	NM_001370089.1:c.115+13311_115+13322del	NM_001370089.1:c.115+13313_115+13322del	NM_001370089.1:c.115+13314_115+13322del	NM_001370089.1:c.115+13315_115+13322del	NM_001370089.1:c.115+13316_115+13322del	NM_001370089.1:c.115+13317_115+13322del	NM_001370089.1:c.115+13318_115+13322del	NM_001370089.1:c.115+13319_115+13322del	NM_001370089.1:c.115+13320_115+13322del	NM_001370089.1:c.115+13321_115+13322del	NM_001370089.1:c.115+13322del	NM_001370089.1:c.115+13322dup	NM_001370089.1:c.115+13321_115+13322dup	NM_001370089.1:c.115+13320_115+13322dup
CARM1 transcript	NM_199141.1:c.220+13967=	NM_199141.1:c.220+13980_220+13992del	NM_199141.1:c.220+13981_220+13992del	NM_199141.1:c.220+13983_220+13992del	NM_199141.1:c.220+13984_220+13992del	NM_199141.1:c.220+13985_220+13992del	NM_199141.1:c.220+13986_220+13992del	NM_199141.1:c.220+13987_220+13992del	NM_199141.1:c.220+13988_220+13992del	NM_199141.1:c.220+13989_220+13992del	NM_199141.1:c.220+13990_220+13992del	NM_199141.1:c.220+13991_220+13992del	NM_199141.1:c.220+13992del	NM_199141.1:c.220+13992dup	NM_199141.1:c.220+13991_220+13992dup	NM_199141.1:c.220+13990_220+13992dup
CARM1 transcript variant 1	NM_199141.2:c.220+13967=	NM_199141.2:c.220+13980_220+13992del	NM_199141.2:c.220+13981_220+13992del	NM_199141.2:c.220+13983_220+13992del	NM_199141.2:c.220+13984_220+13992del	NM_199141.2:c.220+13985_220+13992del	NM_199141.2:c.220+13986_220+13992del	NM_199141.2:c.220+13987_220+13992del	NM_199141.2:c.220+13988_220+13992del	NM_199141.2:c.220+13989_220+13992del	NM_199141.2:c.220+13990_220+13992del	NM_199141.2:c.220+13991_220+13992del	NM_199141.2:c.220+13992del	NM_199141.2:c.220+13992dup	NM_199141.2:c.220+13991_220+13992dup	NM_199141.2:c.220+13990_220+13992dup
CARM1 transcript variant X1	XM_005259708.1:c.220+13967=	XM_005259708.1:c.220+13980_220+13992del	XM_005259708.1:c.220+13981_220+13992del	XM_005259708.1:c.220+13983_220+13992del	XM_005259708.1:c.220+13984_220+13992del	XM_005259708.1:c.220+13985_220+13992del	XM_005259708.1:c.220+13986_220+13992del	XM_005259708.1:c.220+13987_220+13992del	XM_005259708.1:c.220+13988_220+13992del	XM_005259708.1:c.220+13989_220+13992del	XM_005259708.1:c.220+13990_220+13992del	XM_005259708.1:c.220+13991_220+13992del	XM_005259708.1:c.220+13992del	XM_005259708.1:c.220+13992dup	XM_005259708.1:c.220+13991_220+13992dup	XM_005259708.1:c.220+13990_220+13992dup
CARM1 transcript variant X1	XM_047438058.1:c.115+13297=	XM_047438058.1:c.115+13310_115+13322del	XM_047438058.1:c.115+13311_115+13322del	XM_047438058.1:c.115+13313_115+13322del	XM_047438058.1:c.115+13314_115+13322del	XM_047438058.1:c.115+13315_115+13322del	XM_047438058.1:c.115+13316_115+13322del	XM_047438058.1:c.115+13317_115+13322del	XM_047438058.1:c.115+13318_115+13322del	XM_047438058.1:c.115+13319_115+13322del	XM_047438058.1:c.115+13320_115+13322del	XM_047438058.1:c.115+13321_115+13322del	XM_047438058.1:c.115+13322del	XM_047438058.1:c.115+13322dup	XM_047438058.1:c.115+13321_115+13322dup	XM_047438058.1:c.115+13320_115+13322dup

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#.

31 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SWEGEN	ss3017105048	Nov 08, 2017 (151)
2	EVA_DECODE	ss3702351853	Jul 13, 2019 (153)
3	EVA_DECODE	ss3702351855	Jul 13, 2019 (153)
4	EVA_DECODE	ss3702351858	Jul 13, 2019 (153)
5	EVA_DECODE	ss3702351860	Jul 13, 2019 (153)
6	GNOMAD	ss4327712320	Apr 27, 2021 (155)
7	GNOMAD	ss4327712321	Apr 27, 2021 (155)
8	GNOMAD	ss4327712322	Apr 27, 2021 (155)
9	GNOMAD	ss4327712327	Apr 27, 2021 (155)
10	GNOMAD	ss4327712328	Apr 27, 2021 (155)
11	GNOMAD	ss4327712329	Apr 27, 2021 (155)
12	GNOMAD	ss4327712330	Apr 27, 2021 (155)
13	GNOMAD	ss4327712331	Apr 27, 2021 (155)
14	GNOMAD	ss4327712332	Apr 27, 2021 (155)
15	GNOMAD	ss4327712333	Apr 27, 2021 (155)
16	GNOMAD	ss4327712334	Apr 27, 2021 (155)
17	GNOMAD	ss4327712335	Apr 27, 2021 (155)
18	TOPMED	ss5068074107	Apr 27, 2021 (155)
19	TOPMED	ss5068074108	Apr 27, 2021 (155)
20	TOMMO_GENOMICS	ss5226760981	Apr 27, 2021 (155)
21	TOMMO_GENOMICS	ss5226760982	Apr 27, 2021 (155)
22	TOMMO_GENOMICS	ss5226760983	Apr 27, 2021 (155)
23	1000G_HIGH_COVERAGE	ss5306507287	Oct 16, 2022 (156)
24	HUGCELL_USP	ss5499134589	Oct 16, 2022 (156)
25	HUGCELL_USP	ss5499134590	Oct 16, 2022 (156)
26	HUGCELL_USP	ss5499134591	Oct 16, 2022 (156)
27	SANFORD_IMAGENETICS	ss5661983732	Oct 16, 2022 (156)
28	TOMMO_GENOMICS	ss5785047628	Oct 16, 2022 (156)
29	TOMMO_GENOMICS	ss5785047629	Oct 16, 2022 (156)
30	TOMMO_GENOMICS	ss5785047631	Oct 16, 2022 (156)
31	TOMMO_GENOMICS	ss5785047632	Oct 16, 2022 (156)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534167741 (NC_000019.10:10885888::T 22/71980) Row 534167742 (NC_000019.10:10885888::TT 9/71970) Row 534167743 (NC_000019.10:10885888::TTT 3/71978)...	-	Apr 27, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534167741 (NC_000019.10:10885888::T 22/71980) Row 534167742 (NC_000019.10:10885888::TT 9/71970) Row 534167743 (NC_000019.10:10885888::TTT 3/71978)...	-	Apr 27, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534167741 (NC_000019.10:10885888::T 22/71980) Row 534167742 (NC_000019.10:10885888::TT 9/71970) Row 534167743 (NC_000019.10:10885888::TTT 3/71978)...	-	Apr 27, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534167741 (NC_000019.10:10885888::T 22/71980) Row 534167742 (NC_000019.10:10885888::TT 9/71970) Row 534167743 (NC_000019.10:10885888::TTT 3/71978)...	-	Apr 27, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534167741 (NC_000019.10:10885888::T 22/71980) Row 534167742 (NC_000019.10:10885888::TT 9/71970) Row 534167743 (NC_000019.10:10885888::TTT 3/71978)...	-	Apr 27, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534167741 (NC_000019.10:10885888::T 22/71980) Row 534167742 (NC_000019.10:10885888::TT 9/71970) Row 534167743 (NC_000019.10:10885888::TTT 3/71978)...	-	Apr 27, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534167741 (NC_000019.10:10885888::T 22/71980) Row 534167742 (NC_000019.10:10885888::TT 9/71970) Row 534167743 (NC_000019.10:10885888::TTT 3/71978)...	-	Apr 27, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534167741 (NC_000019.10:10885888::T 22/71980) Row 534167742 (NC_000019.10:10885888::TT 9/71970) Row 534167743 (NC_000019.10:10885888::TTT 3/71978)...	-	Apr 27, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534167741 (NC_000019.10:10885888::T 22/71980) Row 534167742 (NC_000019.10:10885888::TT 9/71970) Row 534167743 (NC_000019.10:10885888::TTT 3/71978)...	-	Apr 27, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534167741 (NC_000019.10:10885888::T 22/71980) Row 534167742 (NC_000019.10:10885888::TT 9/71970) Row 534167743 (NC_000019.10:10885888::TTT 3/71978)...	-	Apr 27, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534167741 (NC_000019.10:10885888::T 22/71980) Row 534167742 (NC_000019.10:10885888::TT 9/71970) Row 534167743 (NC_000019.10:10885888::TTT 3/71978)...	-	Apr 27, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 534167741 (NC_000019.10:10885888::T 22/71980) Row 534167742 (NC_000019.10:10885888::TT 9/71970) Row 534167743 (NC_000019.10:10885888::TTT 3/71978)...	-	Apr 27, 2021 (155)
44	8.3KJPN Submission ignored due to conflicting rows: Row 84730288 (NC_000019.9:10996564:T: 4199/14652) Row 84730289 (NC_000019.9:10996564:TT: 9/14652) Row 84730290 (NC_000019.9:10996564:TTTTT: 2/14652)	-	Apr 27, 2021 (155)
45	8.3KJPN Submission ignored due to conflicting rows: Row 84730288 (NC_000019.9:10996564:T: 4199/14652) Row 84730289 (NC_000019.9:10996564:TT: 9/14652) Row 84730290 (NC_000019.9:10996564:TTTTT: 2/14652)	-	Apr 27, 2021 (155)
46	8.3KJPN Submission ignored due to conflicting rows: Row 84730288 (NC_000019.9:10996564:T: 4199/14652) Row 84730289 (NC_000019.9:10996564:TT: 9/14652) Row 84730290 (NC_000019.9:10996564:TTTTT: 2/14652)	-	Apr 27, 2021 (155)
47	14KJPN Submission ignored due to conflicting rows: Row 118884732 (NC_000019.10:10885888:T: 6146/20890) Row 118884733 (NC_000019.10:10885888:TT: 14/20890) Row 118884735 (NC_000019.10:10885888:TTTTT: 1/20890)...	-	Oct 16, 2022 (156)
48	14KJPN Submission ignored due to conflicting rows: Row 118884732 (NC_000019.10:10885888:T: 6146/20890) Row 118884733 (NC_000019.10:10885888:TT: 14/20890) Row 118884735 (NC_000019.10:10885888:TTTTT: 1/20890)...	-	Oct 16, 2022 (156)
49	14KJPN Submission ignored due to conflicting rows: Row 118884732 (NC_000019.10:10885888:T: 6146/20890) Row 118884733 (NC_000019.10:10885888:TT: 14/20890) Row 118884735 (NC_000019.10:10885888:TTTTT: 1/20890)...	-	Oct 16, 2022 (156)
50	14KJPN Submission ignored due to conflicting rows: Row 118884732 (NC_000019.10:10885888:T: 6146/20890) Row 118884733 (NC_000019.10:10885888:TT: 14/20890) Row 118884735 (NC_000019.10:10885888:TTTTT: 1/20890)...	-	Oct 16, 2022 (156)
51	TopMed Submission ignored due to conflicting rows: Row 283619771 (NC_000019.10:10885888:TTTTTTTT: 2/264690) Row 283619772 (NC_000019.10:10885888:TTTTTTTTTTTT: 1/264690)	-	Apr 27, 2021 (155)
52	TopMed Submission ignored due to conflicting rows: Row 283619771 (NC_000019.10:10885888:TTTTTTTT: 2/264690) Row 283619772 (NC_000019.10:10885888:TTTTTTTTTTTT: 1/264690)	-	Apr 27, 2021 (155)
53	ALFA	NC_000019.10 - 10885889	Apr 27, 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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4327712335	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTT:	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
9662467600	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss5068074108	NC_000019.10:10885888:TTTTTTTTTTTT:	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
9662467600	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4327712334, ss5785047632	NC_000019.10:10885888:TTTTTTTTTT:	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
9662467600	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4327712333	NC_000019.10:10885888:TTTTTTTTT:	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
9662467600	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss5068074107	NC_000019.10:10885888:TTTTTTTT:	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
9662467600	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4327712332	NC_000019.10:10885888:TTTTTTT:	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
9662467600	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4327712331	NC_000019.10:10885888:TTTTTT:	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
9662467600	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss5226760983	NC_000019.9:10996564:TTTTT:	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3702351853, ss5785047631	NC_000019.10:10885888:TTTTT:	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4327712330	NC_000019.10:10885888:TTTT:	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
9662467600	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4327712329, ss5499134591	NC_000019.10:10885888:TTT:	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
9662467600	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5226760982	NC_000019.9:10996564:TT:	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4327712328, ss5499134590, ss5785047629	NC_000019.10:10885888:TT:	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
9662467600	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3017105048, ss5226760981, ss5661983732	NC_000019.9:10996564:T:	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4327712327, ss5306507287, ss5499134589, ss5785047628	NC_000019.10:10885888:T:	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9662467600	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3702351855	NC_000019.10:10885892:T:	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4327712320	NC_000019.10:10885888::T	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9662467600	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3702351860	NC_000019.10:10885891::T	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4327712321	NC_000019.10:10885888::TT	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3702351858	NC_000019.10:10885890::TT	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4327712322	NC_000019.10:10885888::TTT	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI
ss2389771572	NC_000019.9:10996564:TTTTTTT:	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT
ss2389771573	NC_000019.9:10996564:TTTTTTTTTT:	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT
ss2389771574	NC_000019.9:10996564:TTTTTTTTTTTT:	NC_000019.10:10885888:TTTTTTTTTTTT… NC_000019.10:10885888:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT

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

No publications for rs766173367

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

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs766173367