Name: rs35754003
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.

rs35754003

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:93464160-93464181 (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)₁₁ / del(T)₈ / del(T)₇ / del…
del(T)₁₁ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / ins(T)₃₇
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.4533 (2270/5008, 1000G)
(T)₂₂=0.2845 (1394/4900, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
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	4900	TTTTTTTTTTTTTTTTTTTTTT=0.2845	TTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0516, TTTTTTTTTTTTTTTTTTTTT=0.4776, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0831, TTTTTTTTTTTTTTTTTTTTTTT=0.0700, TTTTTTTTTTTTTTTTTTTTTTTT=0.0298, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0035	0.227756	0.373174	0.39907	27
European	Sub	4466	TTTTTTTTTTTTTTTTTTTTTT=0.2163	TTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0564, TTTTTTTTTTTTTTTTTTTTT=0.5228, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0911, TTTTTTTTTTTTTTTTTTTTTTT=0.0768, TTTTTTTTTTTTTTTTTTTTTTTT=0.0327, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0038	0.100775	0.434884	0.464341	2
African	Sub	408	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	8	TTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	400	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	2	TTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	2	TTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	2	TTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	2	TTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other	Sub	20	TTTTTTTTTTTTTTTTTTTTTT=0.70	TTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.05, TTTTTTTTTTTTTTTTTTTTT=0.25, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.666667	0.111111	0.222222	1

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	(T)₂₂=0.5467	delT=0.4533
1000Genomes	African	Sub	1322	(T)₂₂=0.8306	delT=0.1694
1000Genomes	East Asian	Sub	1008	(T)₂₂=0.4206	delT=0.5794
1000Genomes	Europe	Sub	1006	(T)₂₂=0.3539	delT=0.6461
1000Genomes	South Asian	Sub	978	(T)₂₂=0.562	delT=0.438
1000Genomes	American	Sub	694	(T)₂₂=0.447	delT=0.553
Allele Frequency Aggregator	Total	Global	4900	(T)₂₂=0.2845	del(T)₁₁=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0516, delT=0.4776, dupT=0.0700, dupTT=0.0298, dupTTT=0.0831, dup(T)₄=0.0035
Allele Frequency Aggregator	European	Sub	4466	(T)₂₂=0.2163	del(T)₁₁=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0564, delT=0.5228, dupT=0.0768, dupTT=0.0327, dupTTT=0.0911, dup(T)₄=0.0038
Allele Frequency Aggregator	African	Sub	408	(T)₂₂=1.000	del(T)₁₁=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Other	Sub	20	(T)₂₂=0.70	del(T)₁₁=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.05, delT=0.25, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	2	(T)₂₂=1.0	del(T)₁₁=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0
Allele Frequency Aggregator	Latin American 2	Sub	2	(T)₂₂=1.0	del(T)₁₁=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0
Allele Frequency Aggregator	Asian	Sub	2	(T)₂₂=1.0	del(T)₁₁=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0
Allele Frequency Aggregator	South Asian	Sub	0	(T)₂₂=0	del(T)₁₁=0, del(T)₈=0, del(T)₇=0, del(T)₆=0, del(T)₅=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0, dup(T)₄=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 15	NC_000015.10:g.93464171_93464181del
GRCh38.p14 chr 15	NC_000015.10:g.93464174_93464181del
GRCh38.p14 chr 15	NC_000015.10:g.93464175_93464181del
GRCh38.p14 chr 15	NC_000015.10:g.93464176_93464181del
GRCh38.p14 chr 15	NC_000015.10:g.93464177_93464181del
GRCh38.p14 chr 15	NC_000015.10:g.93464178_93464181del
GRCh38.p14 chr 15	NC_000015.10:g.93464179_93464181del
GRCh38.p14 chr 15	NC_000015.10:g.93464180_93464181del
GRCh38.p14 chr 15	NC_000015.10:g.93464181del
GRCh38.p14 chr 15	NC_000015.10:g.93464181dup
GRCh38.p14 chr 15	NC_000015.10:g.93464180_93464181dup
GRCh38.p14 chr 15	NC_000015.10:g.93464179_93464181dup
GRCh38.p14 chr 15	NC_000015.10:g.93464178_93464181dup
GRCh38.p14 chr 15	NC_000015.10:g.93464177_93464181dup
GRCh38.p14 chr 15	NC_000015.10:g.93464176_93464181dup
GRCh38.p14 chr 15	NC_000015.10:g.93464175_93464181dup
GRCh38.p14 chr 15	NC_000015.10:g.93464174_93464181dup
GRCh38.p14 chr 15	NC_000015.10:g.93464173_93464181dup
GRCh38.p14 chr 15	NC_000015.10:g.93464172_93464181dup
GRCh38.p14 chr 15	NC_000015.10:g.93464181_93464182insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 15	NC_000015.9:g.94007400_94007410del
GRCh37.p13 chr 15	NC_000015.9:g.94007403_94007410del
GRCh37.p13 chr 15	NC_000015.9:g.94007404_94007410del
GRCh37.p13 chr 15	NC_000015.9:g.94007405_94007410del
GRCh37.p13 chr 15	NC_000015.9:g.94007406_94007410del
GRCh37.p13 chr 15	NC_000015.9:g.94007407_94007410del
GRCh37.p13 chr 15	NC_000015.9:g.94007408_94007410del
GRCh37.p13 chr 15	NC_000015.9:g.94007409_94007410del
GRCh37.p13 chr 15	NC_000015.9:g.94007410del
GRCh37.p13 chr 15	NC_000015.9:g.94007410dup
GRCh37.p13 chr 15	NC_000015.9:g.94007409_94007410dup
GRCh37.p13 chr 15	NC_000015.9:g.94007408_94007410dup
GRCh37.p13 chr 15	NC_000015.9:g.94007407_94007410dup
GRCh37.p13 chr 15	NC_000015.9:g.94007406_94007410dup
GRCh37.p13 chr 15	NC_000015.9:g.94007405_94007410dup
GRCh37.p13 chr 15	NC_000015.9:g.94007404_94007410dup
GRCh37.p13 chr 15	NC_000015.9:g.94007403_94007410dup
GRCh37.p13 chr 15	NC_000015.9:g.94007402_94007410dup
GRCh37.p13 chr 15	NC_000015.9:g.94007401_94007410dup
GRCh37.p13 chr 15	NC_000015.9:g.94007410_94007411insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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)₂₂=	del(T)₁₁	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	ins(T)₃₇
GRCh38.p14 chr 15	NC_000015.10:g.93464160_93464181=	NC_000015.10:g.93464171_93464181del	NC_000015.10:g.93464174_93464181del	NC_000015.10:g.93464175_93464181del	NC_000015.10:g.93464176_93464181del	NC_000015.10:g.93464177_93464181del	NC_000015.10:g.93464178_93464181del	NC_000015.10:g.93464179_93464181del	NC_000015.10:g.93464180_93464181del	NC_000015.10:g.93464181del	NC_000015.10:g.93464181dup	NC_000015.10:g.93464180_93464181dup	NC_000015.10:g.93464179_93464181dup	NC_000015.10:g.93464178_93464181dup	NC_000015.10:g.93464177_93464181dup	NC_000015.10:g.93464176_93464181dup	NC_000015.10:g.93464175_93464181dup	NC_000015.10:g.93464174_93464181dup	NC_000015.10:g.93464173_93464181dup	NC_000015.10:g.93464172_93464181dup	NC_000015.10:g.93464181_93464182insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 15	NC_000015.9:g.94007389_94007410=	NC_000015.9:g.94007400_94007410del	NC_000015.9:g.94007403_94007410del	NC_000015.9:g.94007404_94007410del	NC_000015.9:g.94007405_94007410del	NC_000015.9:g.94007406_94007410del	NC_000015.9:g.94007407_94007410del	NC_000015.9:g.94007408_94007410del	NC_000015.9:g.94007409_94007410del	NC_000015.9:g.94007410del	NC_000015.9:g.94007410dup	NC_000015.9:g.94007409_94007410dup	NC_000015.9:g.94007408_94007410dup	NC_000015.9:g.94007407_94007410dup	NC_000015.9:g.94007406_94007410dup	NC_000015.9:g.94007405_94007410dup	NC_000015.9:g.94007404_94007410dup	NC_000015.9:g.94007403_94007410dup	NC_000015.9:g.94007402_94007410dup	NC_000015.9:g.94007401_94007410dup	NC_000015.9:g.94007410_94007411insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

76 SubSNP, 44 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40552219	Oct 12, 2018 (152)
2	ABI	ss40592229	Mar 15, 2006 (126)
3	HUMANGENOME_JCVI	ss95667433	Feb 13, 2009 (137)
4	PJP	ss294874037	May 09, 2011 (134)
5	SSMP	ss664295849	Apr 01, 2015 (144)
6	1000GENOMES	ss1375317820	Aug 21, 2014 (142)
7	EVA_UK10K_ALSPAC	ss1708410553	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1708410767	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1710682197	Apr 01, 2015 (144)
10	EVA_UK10K_ALSPAC	ss1710682198	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1710682199	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1710682200	Apr 01, 2015 (144)
13	SWEGEN	ss3013779109	Jan 10, 2018 (151)
14	URBANLAB	ss3650422532	Oct 12, 2018 (152)
15	EVA_DECODE	ss3698492458	Jul 13, 2019 (153)
16	EVA_DECODE	ss3698492459	Jul 13, 2019 (153)
17	EVA_DECODE	ss3698492460	Jul 13, 2019 (153)
18	EVA_DECODE	ss3698492461	Jul 13, 2019 (153)
19	EVA_DECODE	ss3698492462	Jul 13, 2019 (153)
20	EVA_DECODE	ss3698492463	Jul 13, 2019 (153)
21	ACPOP	ss3741183811	Jul 13, 2019 (153)
22	ACPOP	ss3741183812	Jul 13, 2019 (153)
23	ACPOP	ss3741183813	Jul 13, 2019 (153)
24	ACPOP	ss3741183814	Jul 13, 2019 (153)
25	ACPOP	ss3741183815	Jul 13, 2019 (153)
26	ACPOP	ss3741183816	Jul 13, 2019 (153)
27	PACBIO	ss3797815152	Jul 13, 2019 (153)
28	KHV_HUMAN_GENOMES	ss3818767539	Jul 13, 2019 (153)
29	EVA	ss3834385017	Apr 27, 2020 (154)
30	GNOMAD	ss4294052710	Apr 26, 2021 (155)
31	GNOMAD	ss4294052711	Apr 26, 2021 (155)
32	GNOMAD	ss4294052712	Apr 26, 2021 (155)
33	GNOMAD	ss4294052713	Apr 26, 2021 (155)
34	GNOMAD	ss4294052714	Apr 26, 2021 (155)
35	GNOMAD	ss4294052715	Apr 26, 2021 (155)
36	GNOMAD	ss4294052716	Apr 26, 2021 (155)
37	GNOMAD	ss4294052717	Apr 26, 2021 (155)
38	GNOMAD	ss4294052718	Apr 26, 2021 (155)
39	GNOMAD	ss4294052719	Apr 26, 2021 (155)
40	GNOMAD	ss4294052721	Apr 26, 2021 (155)
41	GNOMAD	ss4294052722	Apr 26, 2021 (155)
42	GNOMAD	ss4294052723	Apr 26, 2021 (155)
43	GNOMAD	ss4294052724	Apr 26, 2021 (155)
44	GNOMAD	ss4294052725	Apr 26, 2021 (155)
45	GNOMAD	ss4294052726	Apr 26, 2021 (155)
46	GNOMAD	ss4294052727	Apr 26, 2021 (155)
47	GNOMAD	ss4294052728	Apr 26, 2021 (155)
48	GNOMAD	ss4294052729	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5217616111	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5217616112	Apr 26, 2021 (155)
51	TOMMO_GENOMICS	ss5217616113	Apr 26, 2021 (155)
52	TOMMO_GENOMICS	ss5217616114	Apr 26, 2021 (155)
53	TOMMO_GENOMICS	ss5217616115	Apr 26, 2021 (155)
54	TOMMO_GENOMICS	ss5217616116	Apr 26, 2021 (155)
55	1000G_HIGH_COVERAGE	ss5299512717	Oct 16, 2022 (156)
56	1000G_HIGH_COVERAGE	ss5299512718	Oct 16, 2022 (156)
57	1000G_HIGH_COVERAGE	ss5299512719	Oct 16, 2022 (156)
58	1000G_HIGH_COVERAGE	ss5299512720	Oct 16, 2022 (156)
59	1000G_HIGH_COVERAGE	ss5299512721	Oct 16, 2022 (156)
60	1000G_HIGH_COVERAGE	ss5299512722	Oct 16, 2022 (156)
61	HUGCELL_USP	ss5493118415	Oct 16, 2022 (156)
62	HUGCELL_USP	ss5493118416	Oct 16, 2022 (156)
63	HUGCELL_USP	ss5493118417	Oct 16, 2022 (156)
64	HUGCELL_USP	ss5493118418	Oct 16, 2022 (156)
65	HUGCELL_USP	ss5493118419	Oct 16, 2022 (156)
66	HUGCELL_USP	ss5493118420	Oct 16, 2022 (156)
67	TOMMO_GENOMICS	ss5771852244	Oct 16, 2022 (156)
68	TOMMO_GENOMICS	ss5771852245	Oct 16, 2022 (156)
69	TOMMO_GENOMICS	ss5771852246	Oct 16, 2022 (156)
70	TOMMO_GENOMICS	ss5771852247	Oct 16, 2022 (156)
71	TOMMO_GENOMICS	ss5771852248	Oct 16, 2022 (156)
72	TOMMO_GENOMICS	ss5771852249	Oct 16, 2022 (156)
73	EVA	ss5828614728	Oct 16, 2022 (156)
74	EVA	ss5828614729	Oct 16, 2022 (156)
75	EVA	ss5828614730	Oct 16, 2022 (156)
76	EVA	ss5851417378	Oct 16, 2022 (156)
77	1000Genomes	NC_000015.9 - 94007389	Oct 12, 2018 (152)
78	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 37649852 (NC_000015.9:94007389:T: 1685/3854) Row 37649854 (NC_000015.9:94007388:TTT: 674/3854)	-	Oct 12, 2018 (152)
79	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 37649852 (NC_000015.9:94007389:T: 1685/3854) Row 37649854 (NC_000015.9:94007388:TTT: 674/3854)	-	Oct 12, 2018 (152)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477912260 (NC_000015.10:93464159::T 10908/90256) Row 477912261 (NC_000015.10:93464159::TT 3801/90280) Row 477912262 (NC_000015.10:93464159::TTT 7440/90256)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477912260 (NC_000015.10:93464159::T 10908/90256) Row 477912261 (NC_000015.10:93464159::TT 3801/90280) Row 477912262 (NC_000015.10:93464159::TTT 7440/90256)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477912260 (NC_000015.10:93464159::T 10908/90256) Row 477912261 (NC_000015.10:93464159::TT 3801/90280) Row 477912262 (NC_000015.10:93464159::TTT 7440/90256)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477912260 (NC_000015.10:93464159::T 10908/90256) Row 477912261 (NC_000015.10:93464159::TT 3801/90280) Row 477912262 (NC_000015.10:93464159::TTT 7440/90256)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477912260 (NC_000015.10:93464159::T 10908/90256) Row 477912261 (NC_000015.10:93464159::TT 3801/90280) Row 477912262 (NC_000015.10:93464159::TTT 7440/90256)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477912260 (NC_000015.10:93464159::T 10908/90256) Row 477912261 (NC_000015.10:93464159::TT 3801/90280) Row 477912262 (NC_000015.10:93464159::TTT 7440/90256)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477912260 (NC_000015.10:93464159::T 10908/90256) Row 477912261 (NC_000015.10:93464159::TT 3801/90280) Row 477912262 (NC_000015.10:93464159::TTT 7440/90256)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477912260 (NC_000015.10:93464159::T 10908/90256) Row 477912261 (NC_000015.10:93464159::TT 3801/90280) Row 477912262 (NC_000015.10:93464159::TTT 7440/90256)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477912260 (NC_000015.10:93464159::T 10908/90256) Row 477912261 (NC_000015.10:93464159::TT 3801/90280) Row 477912262 (NC_000015.10:93464159::TTT 7440/90256)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477912260 (NC_000015.10:93464159::T 10908/90256) Row 477912261 (NC_000015.10:93464159::TT 3801/90280) Row 477912262 (NC_000015.10:93464159::TTT 7440/90256)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477912260 (NC_000015.10:93464159::T 10908/90256) Row 477912261 (NC_000015.10:93464159::TT 3801/90280) Row 477912262 (NC_000015.10:93464159::TTT 7440/90256)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477912260 (NC_000015.10:93464159::T 10908/90256) Row 477912261 (NC_000015.10:93464159::TT 3801/90280) Row 477912262 (NC_000015.10:93464159::TTT 7440/90256)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477912260 (NC_000015.10:93464159::T 10908/90256) Row 477912261 (NC_000015.10:93464159::TT 3801/90280) Row 477912262 (NC_000015.10:93464159::TTT 7440/90256)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477912260 (NC_000015.10:93464159::T 10908/90256) Row 477912261 (NC_000015.10:93464159::TT 3801/90280) Row 477912262 (NC_000015.10:93464159::TTT 7440/90256)...	-	Apr 26, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477912260 (NC_000015.10:93464159::T 10908/90256) Row 477912261 (NC_000015.10:93464159::TT 3801/90280) Row 477912262 (NC_000015.10:93464159::TTT 7440/90256)...	-	Apr 26, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477912260 (NC_000015.10:93464159::T 10908/90256) Row 477912261 (NC_000015.10:93464159::TT 3801/90280) Row 477912262 (NC_000015.10:93464159::TTT 7440/90256)...	-	Apr 26, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477912260 (NC_000015.10:93464159::T 10908/90256) Row 477912261 (NC_000015.10:93464159::TT 3801/90280) Row 477912262 (NC_000015.10:93464159::TTT 7440/90256)...	-	Apr 26, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477912260 (NC_000015.10:93464159::T 10908/90256) Row 477912261 (NC_000015.10:93464159::TT 3801/90280) Row 477912262 (NC_000015.10:93464159::TTT 7440/90256)...	-	Apr 26, 2021 (155)
98	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477912260 (NC_000015.10:93464159::T 10908/90256) Row 477912261 (NC_000015.10:93464159::TT 3801/90280) Row 477912262 (NC_000015.10:93464159::TTT 7440/90256)...	-	Apr 26, 2021 (155)
99	Northern Sweden Submission ignored due to conflicting rows: Row 14468676 (NC_000015.9:94007388:T: 246/598) Row 14468677 (NC_000015.9:94007388::T 65/598) Row 14468678 (NC_000015.9:94007388:TT: 14/598)...	-	Jul 13, 2019 (153)
100	Northern Sweden Submission ignored due to conflicting rows: Row 14468676 (NC_000015.9:94007388:T: 246/598) Row 14468677 (NC_000015.9:94007388::T 65/598) Row 14468678 (NC_000015.9:94007388:TT: 14/598)...	-	Jul 13, 2019 (153)
101	Northern Sweden Submission ignored due to conflicting rows: Row 14468676 (NC_000015.9:94007388:T: 246/598) Row 14468677 (NC_000015.9:94007388::T 65/598) Row 14468678 (NC_000015.9:94007388:TT: 14/598)...	-	Jul 13, 2019 (153)
102	Northern Sweden Submission ignored due to conflicting rows: Row 14468676 (NC_000015.9:94007388:T: 246/598) Row 14468677 (NC_000015.9:94007388::T 65/598) Row 14468678 (NC_000015.9:94007388:TT: 14/598)...	-	Jul 13, 2019 (153)
103	Northern Sweden Submission ignored due to conflicting rows: Row 14468676 (NC_000015.9:94007388:T: 246/598) Row 14468677 (NC_000015.9:94007388::T 65/598) Row 14468678 (NC_000015.9:94007388:TT: 14/598)...	-	Jul 13, 2019 (153)
104	Northern Sweden Submission ignored due to conflicting rows: Row 14468676 (NC_000015.9:94007388:T: 246/598) Row 14468677 (NC_000015.9:94007388::T 65/598) Row 14468678 (NC_000015.9:94007388:TT: 14/598)...	-	Jul 13, 2019 (153)
105	8.3KJPN Submission ignored due to conflicting rows: Row 75585418 (NC_000015.9:94007388:T: 10204/16630) Row 75585419 (NC_000015.9:94007388::T 2389/16630) Row 75585420 (NC_000015.9:94007388:TT: 59/16630)...	-	Apr 26, 2021 (155)
106	8.3KJPN Submission ignored due to conflicting rows: Row 75585418 (NC_000015.9:94007388:T: 10204/16630) Row 75585419 (NC_000015.9:94007388::T 2389/16630) Row 75585420 (NC_000015.9:94007388:TT: 59/16630)...	-	Apr 26, 2021 (155)
107	8.3KJPN Submission ignored due to conflicting rows: Row 75585418 (NC_000015.9:94007388:T: 10204/16630) Row 75585419 (NC_000015.9:94007388::T 2389/16630) Row 75585420 (NC_000015.9:94007388:TT: 59/16630)...	-	Apr 26, 2021 (155)
108	8.3KJPN Submission ignored due to conflicting rows: Row 75585418 (NC_000015.9:94007388:T: 10204/16630) Row 75585419 (NC_000015.9:94007388::T 2389/16630) Row 75585420 (NC_000015.9:94007388:TT: 59/16630)...	-	Apr 26, 2021 (155)
109	8.3KJPN Submission ignored due to conflicting rows: Row 75585418 (NC_000015.9:94007388:T: 10204/16630) Row 75585419 (NC_000015.9:94007388::T 2389/16630) Row 75585420 (NC_000015.9:94007388:TT: 59/16630)...	-	Apr 26, 2021 (155)
110	8.3KJPN Submission ignored due to conflicting rows: Row 75585418 (NC_000015.9:94007388:T: 10204/16630) Row 75585419 (NC_000015.9:94007388::T 2389/16630) Row 75585420 (NC_000015.9:94007388:TT: 59/16630)...	-	Apr 26, 2021 (155)
111	14KJPN Submission ignored due to conflicting rows: Row 105689348 (NC_000015.10:93464159:T: 18142/28224) Row 105689349 (NC_000015.10:93464159::T 4122/28224) Row 105689350 (NC_000015.10:93464159::TTT 1492/28224)...	-	Oct 16, 2022 (156)
112	14KJPN Submission ignored due to conflicting rows: Row 105689348 (NC_000015.10:93464159:T: 18142/28224) Row 105689349 (NC_000015.10:93464159::T 4122/28224) Row 105689350 (NC_000015.10:93464159::TTT 1492/28224)...	-	Oct 16, 2022 (156)
113	14KJPN Submission ignored due to conflicting rows: Row 105689348 (NC_000015.10:93464159:T: 18142/28224) Row 105689349 (NC_000015.10:93464159::T 4122/28224) Row 105689350 (NC_000015.10:93464159::TTT 1492/28224)...	-	Oct 16, 2022 (156)
114	14KJPN Submission ignored due to conflicting rows: Row 105689348 (NC_000015.10:93464159:T: 18142/28224) Row 105689349 (NC_000015.10:93464159::T 4122/28224) Row 105689350 (NC_000015.10:93464159::TTT 1492/28224)...	-	Oct 16, 2022 (156)
115	14KJPN Submission ignored due to conflicting rows: Row 105689348 (NC_000015.10:93464159:T: 18142/28224) Row 105689349 (NC_000015.10:93464159::T 4122/28224) Row 105689350 (NC_000015.10:93464159::TTT 1492/28224)...	-	Oct 16, 2022 (156)
116	14KJPN Submission ignored due to conflicting rows: Row 105689348 (NC_000015.10:93464159:T: 18142/28224) Row 105689349 (NC_000015.10:93464159::T 4122/28224) Row 105689350 (NC_000015.10:93464159::TTT 1492/28224)...	-	Oct 16, 2022 (156)
117	UK 10K study - Twins Submission ignored due to conflicting rows: Row 37649852 (NC_000015.9:94007389:T: 1581/3708) Row 37649854 (NC_000015.9:94007388:TTT: 626/3708)	-	Oct 12, 2018 (152)
118	UK 10K study - Twins Submission ignored due to conflicting rows: Row 37649852 (NC_000015.9:94007389:TT: 1581/3708) Row 37649853 (NC_000015.9:94007390:T: 1385/3708) Row 37649854 (NC_000015.9:94007388:TTT: 626/3708)	-	Apr 27, 2020 (154)
119	UK 10K study - Twins Submission ignored due to conflicting rows: Row 37649852 (NC_000015.9:94007389:T: 1581/3708) Row 37649854 (NC_000015.9:94007388:TTT: 626/3708)	-	Oct 12, 2018 (152)
120	ALFA	NC_000015.10 - 93464160	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)
rs71132953	May 11, 2012 (137)
rs72008033	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4294052729	NC_000015.10:93464159:TTTTTTTTTTT:	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
4467483552	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4294052728	NC_000015.10:93464159:TTTTTTTT:	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
4467483552	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4294052727	NC_000015.10:93464159:TTTTTTT:	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
4467483552	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4294052726	NC_000015.10:93464159:TTTTTT:	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
4467483552	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4294052725, ss5299512720, ss5493118420	NC_000015.10:93464159:TTTTT:	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
4467483552	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4294052724	NC_000015.10:93464159:TTTT:	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
4467483552	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss1708410553, ss1708410767	NC_000015.9:94007388:TTT:	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3698492458, ss4294052723	NC_000015.10:93464159:TTT:	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
4467483552	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3013779109, ss3741183813, ss5217616113, ss5828614730	NC_000015.9:94007388:TT:	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss1710682197, ss1710682198	NC_000015.9:94007389:TT:	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4294052722, ss5299512721, ss5493118417, ss5771852248	NC_000015.10:93464159:TT:	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
4467483552	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3698492459	NC_000015.10:93464160:TT:	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss294874037	NC_000015.8:91808392:T:	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
67792394, ss1375317820, ss3741183811, ss3797815152, ss3834385017, ss5217616111, ss5828614729	NC_000015.9:94007388:T:	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
	NC_000015.9:94007389:T:	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss1710682199, ss1710682200	NC_000015.9:94007390:T:	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3650422532, ss3818767539, ss4294052721, ss5299512717, ss5493118415, ss5771852244	NC_000015.10:93464159:T:	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
4467483552	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3698492460	NC_000015.10:93464161:T:	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss40592229	NT_010274.17:8972915:T:	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss95667433	NT_010274.17:8972936:T:	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss664295849, ss3741183812, ss5217616112	NC_000015.9:94007388::T	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4294052710, ss5299512718, ss5493118418, ss5771852245	NC_000015.10:93464159::T	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
4467483552	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3698492461	NC_000015.10:93464162::T	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss40552219	NT_010274.17:8972915::T	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3741183815, ss5217616115	NC_000015.9:94007388::TT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4294052711, ss5299512722, ss5493118416, ss5771852247	NC_000015.10:93464159::TT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
4467483552	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3698492462	NC_000015.10:93464162::TT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3741183814, ss5217616114, ss5828614728	NC_000015.9:94007388::TTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4294052712, ss5299512719, ss5493118419, ss5771852246, ss5851417378	NC_000015.10:93464159::TTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4467483552	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3698492463	NC_000015.10:93464162::TTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5217616116	NC_000015.9:94007388::TTTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4294052713, ss5771852249	NC_000015.10:93464159::TTTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4467483552	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4294052714	NC_000015.10:93464159::TTTTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4294052715	NC_000015.10:93464159::TTTTTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4294052716	NC_000015.10:93464159::TTTTTTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4294052717	NC_000015.10:93464159::TTTTTTTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4294052718	NC_000015.10:93464159::TTTTTTTTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4294052719	NC_000015.10:93464159::TTTTTTTTTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3741183816	NC_000015.9:94007388::TTTTTTTTTTTT… NC_000015.9:94007388::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000015.10:93464159:TTTTTTTTTTTT… NC_000015.10:93464159:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs35754003

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

rs35754003