Name: rs55637761
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.

rs55637761

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr13:43863676-43863703 (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(TG)₇ / del(TG)₆ / del(TG)₅ / d…
del(TG)₇ / del(TG)₆ / del(TG)₅ / del(TG)₄ / del(TG)₃ / delTGTG / delTG / dupTG / dupTGTG / dup(TG)₃ / dup(TG)₄ / dup(TG)₅
Variation Type: Indel Insertion and Deletion
Frequency: (TG)₁₄=0.1466 (734/5008, 1000G)
delTGTG=0.4829 (1861/3854, ALSPAC)
del(TG)₇=0.000 (0/208, ALFA) (+ 11 more)
del(TG)₆=0.000 (0/208, ALFA)
del(TG)₅=0.000 (0/208, ALFA)
del(TG)₄=0.000 (0/208, ALFA)
del(TG)₃=0.000 (0/208, ALFA)
delTGTG=0.000 (0/208, ALFA)
delTG=0.000 (0/208, ALFA)
dupTG=0.000 (0/208, ALFA)
dupTGTG=0.000 (0/208, ALFA)
dup(TG)₃=0.000 (0/208, ALFA)
dup(TG)₄=0.000 (0/208, ALFA)
dup(TG)₅=0.000 (0/208, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CCDC122 : 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	Alt HMOZ	HTRZ	HWEP
Total	Global	208	TGTGTGTGTGTGTGTGTGTGTGTGTGTG=1.000	TGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000	1.0	0.0	0.0	N/A
European	Sub	14	TGTGTGTGTGTGTGTGTGTGTGTGTGTG=1.00	TGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00	1.0	0.0	0.0	N/A
African	Sub	152	TGTGTGTGTGTGTGTGTGTGTGTGTGTG=1.000	TGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000	1.0	0.0	0.0	N/A
African Others	Sub	4	TGTGTGTGTGTGTGTGTGTGTGTGTGTG=1.0	TGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0	1.0	0.0	0.0	N/A
African American	Sub	148	TGTGTGTGTGTGTGTGTGTGTGTGTGTG=1.000	TGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.000	1.0	0.0	0.0	N/A
Asian	Sub	6	TGTGTGTGTGTGTGTGTGTGTGTGTGTG=1.0	TGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	6	TGTGTGTGTGTGTGTGTGTGTGTGTGTG=1.0	TGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	TGTGTGTGTGTGTGTGTGTGTGTGTGTG=0	TGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0	0	0	0	N/A
Latin American 1	Sub	0	TGTGTGTGTGTGTGTGTGTGTGTGTGTG=0	TGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0	0	0	0	N/A
Latin American 2	Sub	22	TGTGTGTGTGTGTGTGTGTGTGTGTGTG=1.00	TGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	0	TGTGTGTGTGTGTGTGTGTGTGTGTGTG=0	TGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0	0	0	0	N/A
Other	Sub	14	TGTGTGTGTGTGTGTGTGTGTGTGTGTG=1.00	TGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00, TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG=0.00	1.0	0.0	0.0	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
1000Genomes	Global	Study-wide	5008	(TG)₁₄=0.1466	delTGTG=0.8534
1000Genomes	African	Sub	1322	(TG)₁₄=0.2693	delTGTG=0.7307
1000Genomes	East Asian	Sub	1008	(TG)₁₄=0.2192	delTGTG=0.7808
1000Genomes	Europe	Sub	1006	(TG)₁₄=0.0249	delTGTG=0.9751
1000Genomes	South Asian	Sub	978	(TG)₁₄=0.030	delTGTG=0.970
1000Genomes	American	Sub	694	(TG)₁₄=0.148	delTGTG=0.852
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(TG)₁₄=0.5171	delTGTG=0.4829
Allele Frequency Aggregator	Total	Global	208	(TG)₁₄=1.000	del(TG)₇=0.000, del(TG)₆=0.000, del(TG)₅=0.000, del(TG)₄=0.000, del(TG)₃=0.000, delTGTG=0.000, delTG=0.000, dupTG=0.000, dupTGTG=0.000, dup(TG)₃=0.000, dup(TG)₄=0.000, dup(TG)₅=0.000
Allele Frequency Aggregator	African	Sub	152	(TG)₁₄=1.000	del(TG)₇=0.000, del(TG)₆=0.000, del(TG)₅=0.000, del(TG)₄=0.000, del(TG)₃=0.000, delTGTG=0.000, delTG=0.000, dupTG=0.000, dupTGTG=0.000, dup(TG)₃=0.000, dup(TG)₄=0.000, dup(TG)₅=0.000
Allele Frequency Aggregator	Latin American 2	Sub	22	(TG)₁₄=1.00	del(TG)₇=0.00, del(TG)₆=0.00, del(TG)₅=0.00, del(TG)₄=0.00, del(TG)₃=0.00, delTGTG=0.00, delTG=0.00, dupTG=0.00, dupTGTG=0.00, dup(TG)₃=0.00, dup(TG)₄=0.00, dup(TG)₅=0.00
Allele Frequency Aggregator	European	Sub	14	(TG)₁₄=1.00	del(TG)₇=0.00, del(TG)₆=0.00, del(TG)₅=0.00, del(TG)₄=0.00, del(TG)₃=0.00, delTGTG=0.00, delTG=0.00, dupTG=0.00, dupTGTG=0.00, dup(TG)₃=0.00, dup(TG)₄=0.00, dup(TG)₅=0.00
Allele Frequency Aggregator	Other	Sub	14	(TG)₁₄=1.00	del(TG)₇=0.00, del(TG)₆=0.00, del(TG)₅=0.00, del(TG)₄=0.00, del(TG)₃=0.00, delTGTG=0.00, delTG=0.00, dupTG=0.00, dupTGTG=0.00, dup(TG)₃=0.00, dup(TG)₄=0.00, dup(TG)₅=0.00
Allele Frequency Aggregator	Asian	Sub	6	(TG)₁₄=1.0	del(TG)₇=0.0, del(TG)₆=0.0, del(TG)₅=0.0, del(TG)₄=0.0, del(TG)₃=0.0, delTGTG=0.0, delTG=0.0, dupTG=0.0, dupTGTG=0.0, dup(TG)₃=0.0, dup(TG)₄=0.0, dup(TG)₅=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(TG)₁₄=0	del(TG)₇=0, del(TG)₆=0, del(TG)₅=0, del(TG)₄=0, del(TG)₃=0, delTGTG=0, delTG=0, dupTG=0, dupTGTG=0, dup(TG)₃=0, dup(TG)₄=0, dup(TG)₅=0
Allele Frequency Aggregator	South Asian	Sub	0	(TG)₁₄=0	del(TG)₇=0, del(TG)₆=0, del(TG)₅=0, del(TG)₄=0, del(TG)₃=0, delTGTG=0, delTG=0, dupTG=0, dupTGTG=0, dup(TG)₃=0, dup(TG)₄=0, dup(TG)₅=0

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 13	NC_000013.11:g.43863676TG[7]
GRCh38.p14 chr 13	NC_000013.11:g.43863676TG[8]
GRCh38.p14 chr 13	NC_000013.11:g.43863676TG[9]
GRCh38.p14 chr 13	NC_000013.11:g.43863676TG[10]
GRCh38.p14 chr 13	NC_000013.11:g.43863676TG[11]
GRCh38.p14 chr 13	NC_000013.11:g.43863676TG[12]
GRCh38.p14 chr 13	NC_000013.11:g.43863676TG[13]
GRCh38.p14 chr 13	NC_000013.11:g.43863676TG[15]
GRCh38.p14 chr 13	NC_000013.11:g.43863676TG[16]
GRCh38.p14 chr 13	NC_000013.11:g.43863676TG[17]
GRCh38.p14 chr 13	NC_000013.11:g.43863676TG[18]
GRCh38.p14 chr 13	NC_000013.11:g.43863676TG[19]
GRCh37.p13 chr 13	NC_000013.10:g.44437812TG[7]
GRCh37.p13 chr 13	NC_000013.10:g.44437812TG[8]
GRCh37.p13 chr 13	NC_000013.10:g.44437812TG[9]
GRCh37.p13 chr 13	NC_000013.10:g.44437812TG[10]
GRCh37.p13 chr 13	NC_000013.10:g.44437812TG[11]
GRCh37.p13 chr 13	NC_000013.10:g.44437812TG[12]
GRCh37.p13 chr 13	NC_000013.10:g.44437812TG[13]
GRCh37.p13 chr 13	NC_000013.10:g.44437812TG[15]
GRCh37.p13 chr 13	NC_000013.10:g.44437812TG[16]
GRCh37.p13 chr 13	NC_000013.10:g.44437812TG[17]
GRCh37.p13 chr 13	NC_000013.10:g.44437812TG[18]
GRCh37.p13 chr 13	NC_000013.10:g.44437812TG[19]

Gene: CCDC122, coiled-coil domain containing 122 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CCDC122 transcript variant 2	NM_001350617.2:c.-207-363… NM_001350617.2:c.-207-3633CA[7]	N/A	Intron Variant
CCDC122 transcript variant 3	NM_001350618.2:c.-207-363… NM_001350618.2:c.-207-3633CA[7]	N/A	Intron Variant
CCDC122 transcript variant 1	NM_144974.5:c.157-3633CA[… NM_144974.5:c.157-3633CA[7]	N/A	Intron Variant
CCDC122 transcript variant X1	XM_017020397.3:c.157-3633… XM_017020397.3:c.157-3633CA[7]	N/A	Intron Variant
CCDC122 transcript variant X2	XM_017020398.2:c.157-3633… XM_017020398.2:c.157-3633CA[7]	N/A	Intron Variant
CCDC122 transcript variant X6	XM_024449324.2:c.-207-363… XM_024449324.2:c.-207-3633CA[7]	N/A	Intron Variant
CCDC122 transcript variant X7	XM_024449327.2:c.-207-363… XM_024449327.2:c.-207-3633CA[7]	N/A	Intron Variant
CCDC122 transcript variant X3	XM_047430112.1:c.157-3633… XM_047430112.1:c.157-3633CA[7]	N/A	Intron Variant
CCDC122 transcript variant X4	XM_047430113.1:c.157-3633… XM_047430113.1:c.157-3633CA[7]	N/A	Intron Variant
CCDC122 transcript variant X5	XM_047430114.1:c.157-3633… XM_047430114.1:c.157-3633CA[7]	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	(TG)₁₄=	del(TG)₇	del(TG)₆	del(TG)₅	del(TG)₄	del(TG)₃	delTGTG	delTG	dupTG	dupTGTG	dup(TG)₃	dup(TG)₄	dup(TG)₅
GRCh38.p14 chr 13	NC_000013.11:g.43863676_43863703=	NC_000013.11:g.43863676TG[7]	NC_000013.11:g.43863676TG[8]	NC_000013.11:g.43863676TG[9]	NC_000013.11:g.43863676TG[10]	NC_000013.11:g.43863676TG[11]	NC_000013.11:g.43863676TG[12]	NC_000013.11:g.43863676TG[13]	NC_000013.11:g.43863676TG[15]	NC_000013.11:g.43863676TG[16]	NC_000013.11:g.43863676TG[17]	NC_000013.11:g.43863676TG[18]	NC_000013.11:g.43863676TG[19]
GRCh37.p13 chr 13	NC_000013.10:g.44437812_44437839=	NC_000013.10:g.44437812TG[7]	NC_000013.10:g.44437812TG[8]	NC_000013.10:g.44437812TG[9]	NC_000013.10:g.44437812TG[10]	NC_000013.10:g.44437812TG[11]	NC_000013.10:g.44437812TG[12]	NC_000013.10:g.44437812TG[13]	NC_000013.10:g.44437812TG[15]	NC_000013.10:g.44437812TG[16]	NC_000013.10:g.44437812TG[17]	NC_000013.10:g.44437812TG[18]	NC_000013.10:g.44437812TG[19]
CCDC122 transcript variant 2	NM_001350617.2:c.-207-3606=	NM_001350617.2:c.-207-3633CA[7]	NM_001350617.2:c.-207-3633CA[8]	NM_001350617.2:c.-207-3633CA[9]	NM_001350617.2:c.-207-3633CA[10]	NM_001350617.2:c.-207-3633CA[11]	NM_001350617.2:c.-207-3633CA[12]	NM_001350617.2:c.-207-3633CA[13]	NM_001350617.2:c.-207-3633CA[15]	NM_001350617.2:c.-207-3633CA[16]	NM_001350617.2:c.-207-3633CA[17]	NM_001350617.2:c.-207-3633CA[18]	NM_001350617.2:c.-207-3633CA[19]
CCDC122 transcript variant 3	NM_001350618.2:c.-207-3606=	NM_001350618.2:c.-207-3633CA[7]	NM_001350618.2:c.-207-3633CA[8]	NM_001350618.2:c.-207-3633CA[9]	NM_001350618.2:c.-207-3633CA[10]	NM_001350618.2:c.-207-3633CA[11]	NM_001350618.2:c.-207-3633CA[12]	NM_001350618.2:c.-207-3633CA[13]	NM_001350618.2:c.-207-3633CA[15]	NM_001350618.2:c.-207-3633CA[16]	NM_001350618.2:c.-207-3633CA[17]	NM_001350618.2:c.-207-3633CA[18]	NM_001350618.2:c.-207-3633CA[19]
CCDC122 transcript	NM_144974.3:c.157-3606=	NM_144974.3:c.157-3633CA[7]	NM_144974.3:c.157-3633CA[8]	NM_144974.3:c.157-3633CA[9]	NM_144974.3:c.157-3633CA[10]	NM_144974.3:c.157-3633CA[11]	NM_144974.3:c.157-3633CA[12]	NM_144974.3:c.157-3633CA[13]	NM_144974.3:c.157-3633CA[15]	NM_144974.3:c.157-3633CA[16]	NM_144974.3:c.157-3633CA[17]	NM_144974.3:c.157-3633CA[18]	NM_144974.3:c.157-3633CA[19]
CCDC122 transcript variant 1	NM_144974.5:c.157-3606=	NM_144974.5:c.157-3633CA[7]	NM_144974.5:c.157-3633CA[8]	NM_144974.5:c.157-3633CA[9]	NM_144974.5:c.157-3633CA[10]	NM_144974.5:c.157-3633CA[11]	NM_144974.5:c.157-3633CA[12]	NM_144974.5:c.157-3633CA[13]	NM_144974.5:c.157-3633CA[15]	NM_144974.5:c.157-3633CA[16]	NM_144974.5:c.157-3633CA[17]	NM_144974.5:c.157-3633CA[18]	NM_144974.5:c.157-3633CA[19]
CCDC122 transcript variant X1	XM_005266272.1:c.157-3606=	XM_005266272.1:c.157-3633CA[7]	XM_005266272.1:c.157-3633CA[8]	XM_005266272.1:c.157-3633CA[9]	XM_005266272.1:c.157-3633CA[10]	XM_005266272.1:c.157-3633CA[11]	XM_005266272.1:c.157-3633CA[12]	XM_005266272.1:c.157-3633CA[13]	XM_005266272.1:c.157-3633CA[15]	XM_005266272.1:c.157-3633CA[16]	XM_005266272.1:c.157-3633CA[17]	XM_005266272.1:c.157-3633CA[18]	XM_005266272.1:c.157-3633CA[19]
CCDC122 transcript variant X2	XM_005266273.1:c.-207-3606=	XM_005266273.1:c.-207-3633CA[7]	XM_005266273.1:c.-207-3633CA[8]	XM_005266273.1:c.-207-3633CA[9]	XM_005266273.1:c.-207-3633CA[10]	XM_005266273.1:c.-207-3633CA[11]	XM_005266273.1:c.-207-3633CA[12]	XM_005266273.1:c.-207-3633CA[13]	XM_005266273.1:c.-207-3633CA[15]	XM_005266273.1:c.-207-3633CA[16]	XM_005266273.1:c.-207-3633CA[17]	XM_005266273.1:c.-207-3633CA[18]	XM_005266273.1:c.-207-3633CA[19]
CCDC122 transcript variant X1	XM_017020397.3:c.157-3606=	XM_017020397.3:c.157-3633CA[7]	XM_017020397.3:c.157-3633CA[8]	XM_017020397.3:c.157-3633CA[9]	XM_017020397.3:c.157-3633CA[10]	XM_017020397.3:c.157-3633CA[11]	XM_017020397.3:c.157-3633CA[12]	XM_017020397.3:c.157-3633CA[13]	XM_017020397.3:c.157-3633CA[15]	XM_017020397.3:c.157-3633CA[16]	XM_017020397.3:c.157-3633CA[17]	XM_017020397.3:c.157-3633CA[18]	XM_017020397.3:c.157-3633CA[19]
CCDC122 transcript variant X2	XM_017020398.2:c.157-3606=	XM_017020398.2:c.157-3633CA[7]	XM_017020398.2:c.157-3633CA[8]	XM_017020398.2:c.157-3633CA[9]	XM_017020398.2:c.157-3633CA[10]	XM_017020398.2:c.157-3633CA[11]	XM_017020398.2:c.157-3633CA[12]	XM_017020398.2:c.157-3633CA[13]	XM_017020398.2:c.157-3633CA[15]	XM_017020398.2:c.157-3633CA[16]	XM_017020398.2:c.157-3633CA[17]	XM_017020398.2:c.157-3633CA[18]	XM_017020398.2:c.157-3633CA[19]
CCDC122 transcript variant X6	XM_024449324.2:c.-207-3606=	XM_024449324.2:c.-207-3633CA[7]	XM_024449324.2:c.-207-3633CA[8]	XM_024449324.2:c.-207-3633CA[9]	XM_024449324.2:c.-207-3633CA[10]	XM_024449324.2:c.-207-3633CA[11]	XM_024449324.2:c.-207-3633CA[12]	XM_024449324.2:c.-207-3633CA[13]	XM_024449324.2:c.-207-3633CA[15]	XM_024449324.2:c.-207-3633CA[16]	XM_024449324.2:c.-207-3633CA[17]	XM_024449324.2:c.-207-3633CA[18]	XM_024449324.2:c.-207-3633CA[19]
CCDC122 transcript variant X7	XM_024449327.2:c.-207-3606=	XM_024449327.2:c.-207-3633CA[7]	XM_024449327.2:c.-207-3633CA[8]	XM_024449327.2:c.-207-3633CA[9]	XM_024449327.2:c.-207-3633CA[10]	XM_024449327.2:c.-207-3633CA[11]	XM_024449327.2:c.-207-3633CA[12]	XM_024449327.2:c.-207-3633CA[13]	XM_024449327.2:c.-207-3633CA[15]	XM_024449327.2:c.-207-3633CA[16]	XM_024449327.2:c.-207-3633CA[17]	XM_024449327.2:c.-207-3633CA[18]	XM_024449327.2:c.-207-3633CA[19]
CCDC122 transcript variant X3	XM_047430112.1:c.157-3606=	XM_047430112.1:c.157-3633CA[7]	XM_047430112.1:c.157-3633CA[8]	XM_047430112.1:c.157-3633CA[9]	XM_047430112.1:c.157-3633CA[10]	XM_047430112.1:c.157-3633CA[11]	XM_047430112.1:c.157-3633CA[12]	XM_047430112.1:c.157-3633CA[13]	XM_047430112.1:c.157-3633CA[15]	XM_047430112.1:c.157-3633CA[16]	XM_047430112.1:c.157-3633CA[17]	XM_047430112.1:c.157-3633CA[18]	XM_047430112.1:c.157-3633CA[19]
CCDC122 transcript variant X4	XM_047430113.1:c.157-3606=	XM_047430113.1:c.157-3633CA[7]	XM_047430113.1:c.157-3633CA[8]	XM_047430113.1:c.157-3633CA[9]	XM_047430113.1:c.157-3633CA[10]	XM_047430113.1:c.157-3633CA[11]	XM_047430113.1:c.157-3633CA[12]	XM_047430113.1:c.157-3633CA[13]	XM_047430113.1:c.157-3633CA[15]	XM_047430113.1:c.157-3633CA[16]	XM_047430113.1:c.157-3633CA[17]	XM_047430113.1:c.157-3633CA[18]	XM_047430113.1:c.157-3633CA[19]
CCDC122 transcript variant X5	XM_047430114.1:c.157-3606=	XM_047430114.1:c.157-3633CA[7]	XM_047430114.1:c.157-3633CA[8]	XM_047430114.1:c.157-3633CA[9]	XM_047430114.1:c.157-3633CA[10]	XM_047430114.1:c.157-3633CA[11]	XM_047430114.1:c.157-3633CA[12]	XM_047430114.1:c.157-3633CA[13]	XM_047430114.1:c.157-3633CA[15]	XM_047430114.1:c.157-3633CA[16]	XM_047430114.1:c.157-3633CA[17]	XM_047430114.1:c.157-3633CA[18]	XM_047430114.1:c.157-3633CA[19]

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#.

81 SubSNP, 29 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss77865363	Sep 08, 2015 (146)
2	HGSV	ss77875760	Sep 08, 2015 (146)
3	HGSV	ss77943215	Sep 08, 2015 (146)
4	HGSV	ss82673917	Sep 08, 2015 (146)
5	HUMANGENOME_JCVI	ss95618980	Dec 05, 2013 (138)
6	GMI	ss289174848	May 04, 2012 (137)
7	GMI	ss289174849	May 04, 2012 (137)
8	PJP	ss294795065	May 09, 2011 (137)
9	PJP	ss294795066	May 09, 2011 (135)
10	PJP	ss294795067	May 09, 2011 (135)
11	1000GENOMES	ss327521356	May 09, 2011 (137)
12	1000GENOMES	ss327622701	May 09, 2011 (137)
13	1000GENOMES	ss328069003	May 09, 2011 (137)
14	LUNTER	ss552287581	Apr 25, 2013 (138)
15	LUNTER	ss552593189	Apr 25, 2013 (138)
16	LUNTER	ss553517506	Apr 25, 2013 (138)
17	BILGI_BIOE	ss666597440	Apr 25, 2013 (138)
18	1000GENOMES	ss1373103458	Aug 21, 2014 (142)
19	EVA_UK10K_ALSPAC	ss1707768064	Apr 01, 2015 (144)
20	EVA_UK10K_TWINSUK	ss1707768541	Apr 01, 2015 (144)
21	EVA_UK10K_TWINSUK	ss1710599855	Apr 01, 2015 (144)
22	EVA_UK10K_ALSPAC	ss1710599874	Apr 01, 2015 (144)
23	SWEGEN	ss3010949298	Nov 08, 2017 (151)
24	MCHAISSO	ss3063762986	Nov 08, 2017 (151)
25	MCHAISSO	ss3064594126	Nov 08, 2017 (151)
26	MCHAISSO	ss3065518118	Nov 08, 2017 (151)
27	URBANLAB	ss3650023877	Oct 12, 2018 (152)
28	EVA_DECODE	ss3695203883	Jul 13, 2019 (153)
29	EVA_DECODE	ss3695203884	Jul 13, 2019 (153)
30	EVA_DECODE	ss3695203885	Jul 13, 2019 (153)
31	EVA_DECODE	ss3695203886	Jul 13, 2019 (153)
32	EVA_DECODE	ss3695203887	Jul 13, 2019 (153)
33	INMEGENXS	ss3745599948	Jul 13, 2019 (153)
34	PACBIO	ss3787446290	Jul 13, 2019 (153)
35	PACBIO	ss3787446291	Jul 13, 2019 (153)
36	PACBIO	ss3792514519	Jul 13, 2019 (153)
37	PACBIO	ss3792514520	Jul 13, 2019 (153)
38	PACBIO	ss3797398280	Jul 13, 2019 (153)
39	PACBIO	ss3797398281	Jul 13, 2019 (153)
40	KHV_HUMAN_GENOMES	ss3816742105	Jul 13, 2019 (153)
41	EVA	ss3833524660	Apr 27, 2020 (154)
42	EVA	ss3845828410	Apr 27, 2020 (154)
43	KOGIC	ss3973476237	Apr 27, 2020 (154)
44	KOGIC	ss3973476238	Apr 27, 2020 (154)
45	KOGIC	ss3973476239	Apr 27, 2020 (154)
46	KOGIC	ss3973476240	Apr 27, 2020 (154)
47	GNOMAD	ss4265086150	Apr 26, 2021 (155)
48	GNOMAD	ss4265086151	Apr 26, 2021 (155)
49	GNOMAD	ss4265086152	Apr 26, 2021 (155)
50	GNOMAD	ss4265086153	Apr 26, 2021 (155)
51	GNOMAD	ss4265086154	Apr 26, 2021 (155)
52	GNOMAD	ss4265086155	Apr 26, 2021 (155)
53	GNOMAD	ss4265086156	Apr 26, 2021 (155)
54	GNOMAD	ss4265086157	Apr 26, 2021 (155)
55	GNOMAD	ss4265086158	Apr 26, 2021 (155)
56	GNOMAD	ss4265086159	Apr 26, 2021 (155)
57	TOMMO_GENOMICS	ss5209796638	Apr 26, 2021 (155)
58	TOMMO_GENOMICS	ss5209796639	Apr 26, 2021 (155)
59	TOMMO_GENOMICS	ss5209796640	Apr 26, 2021 (155)
60	TOMMO_GENOMICS	ss5209796641	Apr 26, 2021 (155)
61	TOMMO_GENOMICS	ss5209796642	Apr 26, 2021 (155)
62	1000G_HIGH_COVERAGE	ss5293581934	Oct 17, 2022 (156)
63	1000G_HIGH_COVERAGE	ss5293581935	Oct 17, 2022 (156)
64	1000G_HIGH_COVERAGE	ss5293581936	Oct 17, 2022 (156)
65	1000G_HIGH_COVERAGE	ss5293581937	Oct 17, 2022 (156)
66	1000G_HIGH_COVERAGE	ss5293581938	Oct 17, 2022 (156)
67	1000G_HIGH_COVERAGE	ss5293581939	Oct 17, 2022 (156)
68	HUGCELL_USP	ss5487960302	Oct 17, 2022 (156)
69	HUGCELL_USP	ss5487960303	Oct 17, 2022 (156)
70	HUGCELL_USP	ss5487960304	Oct 17, 2022 (156)
71	HUGCELL_USP	ss5487960305	Oct 17, 2022 (156)
72	HUGCELL_USP	ss5487960306	Oct 17, 2022 (156)
73	EVA	ss5510957735	Oct 17, 2022 (156)
74	TOMMO_GENOMICS	ss5761614163	Oct 17, 2022 (156)
75	TOMMO_GENOMICS	ss5761614164	Oct 17, 2022 (156)
76	TOMMO_GENOMICS	ss5761614165	Oct 17, 2022 (156)
77	TOMMO_GENOMICS	ss5761614166	Oct 17, 2022 (156)
78	TOMMO_GENOMICS	ss5761614167	Oct 17, 2022 (156)
79	EVA	ss5839415345	Oct 17, 2022 (156)
80	EVA	ss5839415346	Oct 17, 2022 (156)
81	EVA	ss5839415347	Oct 17, 2022 (156)
82	1000Genomes	NC_000013.10 - 44437812	Oct 12, 2018 (152)
83	The Avon Longitudinal Study of Parents and Children	NC_000013.10 - 44437812	Oct 12, 2018 (152)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429455148 (NC_000013.11:43863675::TG 1016/137672) Row 429455149 (NC_000013.11:43863675::TGTG 21/137688) Row 429455150 (NC_000013.11:43863675::TGTGTG 623/137684)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429455148 (NC_000013.11:43863675::TG 1016/137672) Row 429455149 (NC_000013.11:43863675::TGTG 21/137688) Row 429455150 (NC_000013.11:43863675::TGTGTG 623/137684)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429455148 (NC_000013.11:43863675::TG 1016/137672) Row 429455149 (NC_000013.11:43863675::TGTG 21/137688) Row 429455150 (NC_000013.11:43863675::TGTGTG 623/137684)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429455148 (NC_000013.11:43863675::TG 1016/137672) Row 429455149 (NC_000013.11:43863675::TGTG 21/137688) Row 429455150 (NC_000013.11:43863675::TGTGTG 623/137684)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429455148 (NC_000013.11:43863675::TG 1016/137672) Row 429455149 (NC_000013.11:43863675::TGTG 21/137688) Row 429455150 (NC_000013.11:43863675::TGTGTG 623/137684)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429455148 (NC_000013.11:43863675::TG 1016/137672) Row 429455149 (NC_000013.11:43863675::TGTG 21/137688) Row 429455150 (NC_000013.11:43863675::TGTGTG 623/137684)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429455148 (NC_000013.11:43863675::TG 1016/137672) Row 429455149 (NC_000013.11:43863675::TGTG 21/137688) Row 429455150 (NC_000013.11:43863675::TGTGTG 623/137684)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429455148 (NC_000013.11:43863675::TG 1016/137672) Row 429455149 (NC_000013.11:43863675::TGTG 21/137688) Row 429455150 (NC_000013.11:43863675::TGTGTG 623/137684)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429455148 (NC_000013.11:43863675::TG 1016/137672) Row 429455149 (NC_000013.11:43863675::TGTG 21/137688) Row 429455150 (NC_000013.11:43863675::TGTGTG 623/137684)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429455148 (NC_000013.11:43863675::TG 1016/137672) Row 429455149 (NC_000013.11:43863675::TGTG 21/137688) Row 429455150 (NC_000013.11:43863675::TGTGTG 623/137684)...	-	Apr 26, 2021 (155)
94	Korean Genome Project Submission ignored due to conflicting rows: Row 29854238 (NC_000013.11:43863677:TGTG: 897/1832) Row 29854239 (NC_000013.11:43863675:TGTGTG: 77/1832) Row 29854240 (NC_000013.11:43863681::TG 70/1832)...	-	Apr 27, 2020 (154)
95	Korean Genome Project Submission ignored due to conflicting rows: Row 29854238 (NC_000013.11:43863677:TGTG: 897/1832) Row 29854239 (NC_000013.11:43863675:TGTGTG: 77/1832) Row 29854240 (NC_000013.11:43863681::TG 70/1832)...	-	Apr 27, 2020 (154)
96	Korean Genome Project Submission ignored due to conflicting rows: Row 29854238 (NC_000013.11:43863677:TGTG: 897/1832) Row 29854239 (NC_000013.11:43863675:TGTGTG: 77/1832) Row 29854240 (NC_000013.11:43863681::TG 70/1832)...	-	Apr 27, 2020 (154)
97	Korean Genome Project Submission ignored due to conflicting rows: Row 29854238 (NC_000013.11:43863677:TGTG: 897/1832) Row 29854239 (NC_000013.11:43863675:TGTGTG: 77/1832) Row 29854240 (NC_000013.11:43863681::TG 70/1832)...	-	Apr 27, 2020 (154)
98	8.3KJPN Submission ignored due to conflicting rows: Row 67765945 (NC_000013.10:44437811:TGTG: 8839/16760) Row 67765946 (NC_000013.10:44437811:TG: 5318/16760) Row 67765947 (NC_000013.10:44437811:TGTGTG: 64/16760)...	-	Apr 26, 2021 (155)
99	8.3KJPN Submission ignored due to conflicting rows: Row 67765945 (NC_000013.10:44437811:TGTG: 8839/16760) Row 67765946 (NC_000013.10:44437811:TG: 5318/16760) Row 67765947 (NC_000013.10:44437811:TGTGTG: 64/16760)...	-	Apr 26, 2021 (155)
100	8.3KJPN Submission ignored due to conflicting rows: Row 67765945 (NC_000013.10:44437811:TGTG: 8839/16760) Row 67765946 (NC_000013.10:44437811:TG: 5318/16760) Row 67765947 (NC_000013.10:44437811:TGTGTG: 64/16760)...	-	Apr 26, 2021 (155)
101	8.3KJPN Submission ignored due to conflicting rows: Row 67765945 (NC_000013.10:44437811:TGTG: 8839/16760) Row 67765946 (NC_000013.10:44437811:TG: 5318/16760) Row 67765947 (NC_000013.10:44437811:TGTGTG: 64/16760)...	-	Apr 26, 2021 (155)
102	8.3KJPN Submission ignored due to conflicting rows: Row 67765945 (NC_000013.10:44437811:TGTG: 8839/16760) Row 67765946 (NC_000013.10:44437811:TG: 5318/16760) Row 67765947 (NC_000013.10:44437811:TGTGTG: 64/16760)...	-	Apr 26, 2021 (155)
103	14KJPN Submission ignored due to conflicting rows: Row 95451267 (NC_000013.11:43863675:TG: 8970/28258) Row 95451268 (NC_000013.11:43863675:TGTG: 14908/28258) Row 95451269 (NC_000013.11:43863675::TG 687/28258)...	-	Oct 17, 2022 (156)
104	14KJPN Submission ignored due to conflicting rows: Row 95451267 (NC_000013.11:43863675:TG: 8970/28258) Row 95451268 (NC_000013.11:43863675:TGTG: 14908/28258) Row 95451269 (NC_000013.11:43863675::TG 687/28258)...	-	Oct 17, 2022 (156)
105	14KJPN Submission ignored due to conflicting rows: Row 95451267 (NC_000013.11:43863675:TG: 8970/28258) Row 95451268 (NC_000013.11:43863675:TGTG: 14908/28258) Row 95451269 (NC_000013.11:43863675::TG 687/28258)...	-	Oct 17, 2022 (156)
106	14KJPN Submission ignored due to conflicting rows: Row 95451267 (NC_000013.11:43863675:TG: 8970/28258) Row 95451268 (NC_000013.11:43863675:TGTG: 14908/28258) Row 95451269 (NC_000013.11:43863675::TG 687/28258)...	-	Oct 17, 2022 (156)
107	14KJPN Submission ignored due to conflicting rows: Row 95451267 (NC_000013.11:43863675:TG: 8970/28258) Row 95451268 (NC_000013.11:43863675:TGTG: 14908/28258) Row 95451269 (NC_000013.11:43863675::TG 687/28258)...	-	Oct 17, 2022 (156)
108	UK 10K study - Twins Submission ignored due to conflicting rows: Row 33839107 (NC_000013.10:44437813:TG: 1903/3708) Row 33839108 (NC_000013.10:44437811:TGTG: 1729/3708)	-	Apr 27, 2020 (154)
109	UK 10K study - Twins	-	Oct 12, 2018 (152)
110	ALFA	NC_000013.11 - 43863676	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)
rs58594522	May 24, 2008 (130)
rs71763862	May 11, 2012 (137)
rs144463002	May 11, 2012 (137)
rs150805538	Sep 17, 2011 (135)
rs72420058	May 11, 2012 (137)
rs139199624	Sep 17, 2011 (135)
rs141832631	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
4944774908	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTG	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTG	(self)
ss4265086159	NC_000013.11:43863675:TGTGTGTGTGTG:	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTG	(self)
4944774908	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTG	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTG	(self)
ss4265086158	NC_000013.11:43863675:TGTGTGTGTG:	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTG	(self)
4944774908	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTG	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTG	(self)
ss3745599948	NC_000013.10:44437811:TGTGTGTG:	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTG	(self)
ss3695203883, ss4265086157, ss5293581939	NC_000013.11:43863675:TGTGTGTG:	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTG	(self)
4944774908	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTG	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTG	(self)
ss5209796640, ss5839415347	NC_000013.10:44437811:TGTGTG:	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTG	(self)
ss3973476238, ss4265086156, ss5293581936, ss5487960302, ss5761614166	NC_000013.11:43863675:TGTGTG:	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTG	(self)
4944774908	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTG	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTG	(self)
ss3695203884	NC_000013.11:43863677:TGTGTG:	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTG	(self)
ss289174849, ss327521356, ss327622701, ss328069003, ss552593189, ss553517506	NC_000013.9:43335811:TGTG:	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss77865363, ss77943215, ss82673917, ss294795066	NC_000013.9:43335835:TGTG:	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTG	(self)
60914315, 33839108, ss666597440, ss1373103458, ss1707768064, ss1707768541, ss3010949298, ss5209796638, ss5510957735, ss5839415345	NC_000013.10:44437811:TGTG:	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss3063762986, ss3064594126, ss3065518118, ss3816742105, ss4265086155, ss5293581934, ss5487960303, ss5761614164	NC_000013.11:43863675:TGTG:	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTG	(self)
4944774908	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTG	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss3973476237	NC_000013.11:43863677:TGTG:	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss3695203885	NC_000013.11:43863679:TGTG:	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss289174848, ss294795065, ss552287581	NC_000013.9:43335811:TG:	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss77875760, ss294795067	NC_000013.9:43335837:TG:	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss3787446290, ss3792514519, ss3797398280, ss3833524660, ss5209796639, ss5839415346	NC_000013.10:44437811:TG:	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss1710599855, ss1710599874	NC_000013.10:44437813:TG:	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss3845828410, ss4265086154, ss5293581935, ss5487960304, ss5761614163	NC_000013.11:43863675:TG:	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
4944774908	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTG	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss3973476240	NC_000013.11:43863679:TG:	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss3695203886	NC_000013.11:43863681:TG:	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss3650023877	NC_000013.11:43863698:GT:	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss95618980	NT_024524.14:25417837:TG:	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss3787446291, ss3792514520, ss3797398281, ss5209796641	NC_000013.10:44437811::TG	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss4265086150, ss5293581937, ss5487960306, ss5761614165	NC_000013.11:43863675::TG	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
4944774908	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss3973476239	NC_000013.11:43863681::TG	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss3695203887	NC_000013.11:43863683::TG	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss5209796642	NC_000013.10:44437811::TGTG	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss4265086151, ss5761614167	NC_000013.11:43863675::TGTG	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
4944774908	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss4265086152, ss5293581938, ss5487960305	NC_000013.11:43863675::TGTGTG	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
4944774908	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
4944774908	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
ss4265086153	NC_000013.11:43863675::TGTGTGTGTG	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)
4944774908	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3191539996	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTG:	NC_000013.11:43863675:TGTGTGTGTGTG… NC_000013.11:43863675:TGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTG

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

No publications for rs55637761

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

rs55637761