Name: rs969908382
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.

rs969908382

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:73206788-73206812 (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)₁₂ / del(T)₁₁ / del(T)₁₀ / d…
del(T)₁₂ / del(T)₁₁ / 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 / dup(T)₄ / dup(T)₅ / dup(T)₆ / ins(T)₄₆
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₂=0.000019 (5/264690, TOPMED)
dupT=0.0516 (448/8688, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NOTO : 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	8688	TTTTTTTTTTTTTTTTTTTTTTTTT=0.8879	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0342, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0516, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0246, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0017, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.923434	0.016757	0.059809	32
European	Sub	7784	TTTTTTTTTTTTTTTTTTTTTTTTT=0.8751	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0382, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0574, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0274, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0019, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.913652	0.018961	0.067386	32
African	Sub	264	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	6	TTTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	258	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	46	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	34	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	12	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	54	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	334	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	40	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	166	TTTTTTTTTTTTTTTTTTTTTTTTT=0.988	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.006, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.006, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	0.987805	0.0	0.012195	0

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
TopMed	Global	Study-wide	264690	(T)₂₅=0.999981	del(T)₁₂=0.000019
Allele Frequency Aggregator	Total	Global	8688	(T)₂₅=0.8879	del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=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=0.0000, delT=0.0342, dupT=0.0516, dupTT=0.0246, dupTTT=0.0017, dup(T)₄=0.0000
Allele Frequency Aggregator	European	Sub	7784	(T)₂₅=0.8751	del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=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=0.0000, delT=0.0382, dupT=0.0574, dupTT=0.0274, dupTTT=0.0019, dup(T)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	334	(T)₂₅=1.000	del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=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	African	Sub	264	(T)₂₅=1.000	del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=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	166	(T)₂₅=0.988	del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=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=0.006, dupTT=0.006, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	54	(T)₂₅=1.00	del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=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=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	Asian	Sub	46	(T)₂₅=1.00	del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=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=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	40	(T)₂₅=1.00	del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=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=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=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 2	NC_000002.12:g.73206801_73206812del
GRCh38.p14 chr 2	NC_000002.12:g.73206802_73206812del
GRCh38.p14 chr 2	NC_000002.12:g.73206803_73206812del
GRCh38.p14 chr 2	NC_000002.12:g.73206804_73206812del
GRCh38.p14 chr 2	NC_000002.12:g.73206805_73206812del
GRCh38.p14 chr 2	NC_000002.12:g.73206806_73206812del
GRCh38.p14 chr 2	NC_000002.12:g.73206807_73206812del
GRCh38.p14 chr 2	NC_000002.12:g.73206808_73206812del
GRCh38.p14 chr 2	NC_000002.12:g.73206809_73206812del
GRCh38.p14 chr 2	NC_000002.12:g.73206810_73206812del
GRCh38.p14 chr 2	NC_000002.12:g.73206811_73206812del
GRCh38.p14 chr 2	NC_000002.12:g.73206812del
GRCh38.p14 chr 2	NC_000002.12:g.73206812dup
GRCh38.p14 chr 2	NC_000002.12:g.73206811_73206812dup
GRCh38.p14 chr 2	NC_000002.12:g.73206810_73206812dup
GRCh38.p14 chr 2	NC_000002.12:g.73206809_73206812dup
GRCh38.p14 chr 2	NC_000002.12:g.73206808_73206812dup
GRCh38.p14 chr 2	NC_000002.12:g.73206807_73206812dup
GRCh38.p14 chr 2	NC_000002.12:g.73206812_73206813insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 2	NC_000002.11:g.73433929_73433940del
GRCh37.p13 chr 2	NC_000002.11:g.73433930_73433940del
GRCh37.p13 chr 2	NC_000002.11:g.73433931_73433940del
GRCh37.p13 chr 2	NC_000002.11:g.73433932_73433940del
GRCh37.p13 chr 2	NC_000002.11:g.73433933_73433940del
GRCh37.p13 chr 2	NC_000002.11:g.73433934_73433940del
GRCh37.p13 chr 2	NC_000002.11:g.73433935_73433940del
GRCh37.p13 chr 2	NC_000002.11:g.73433936_73433940del
GRCh37.p13 chr 2	NC_000002.11:g.73433937_73433940del
GRCh37.p13 chr 2	NC_000002.11:g.73433938_73433940del
GRCh37.p13 chr 2	NC_000002.11:g.73433939_73433940del
GRCh37.p13 chr 2	NC_000002.11:g.73433940del
GRCh37.p13 chr 2	NC_000002.11:g.73433940dup
GRCh37.p13 chr 2	NC_000002.11:g.73433939_73433940dup
GRCh37.p13 chr 2	NC_000002.11:g.73433938_73433940dup
GRCh37.p13 chr 2	NC_000002.11:g.73433937_73433940dup
GRCh37.p13 chr 2	NC_000002.11:g.73433936_73433940dup
GRCh37.p13 chr 2	NC_000002.11:g.73433935_73433940dup
GRCh37.p13 chr 2	NC_000002.11:g.73433940_73433941insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: NOTO, notochord homeobox (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NOTO transcript	NM_001134462.2:c.383-1599… NM_001134462.2:c.383-1599_383-1588del	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	(T)₂₅=	del(T)₁₂	del(T)₁₁	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	dup(T)₄	dup(T)₅	dup(T)₆	ins(T)₄₆
GRCh38.p14 chr 2	NC_000002.12:g.73206788_73206812=	NC_000002.12:g.73206801_73206812del	NC_000002.12:g.73206802_73206812del	NC_000002.12:g.73206803_73206812del	NC_000002.12:g.73206804_73206812del	NC_000002.12:g.73206805_73206812del	NC_000002.12:g.73206806_73206812del	NC_000002.12:g.73206807_73206812del	NC_000002.12:g.73206808_73206812del	NC_000002.12:g.73206809_73206812del	NC_000002.12:g.73206810_73206812del	NC_000002.12:g.73206811_73206812del	NC_000002.12:g.73206812del	NC_000002.12:g.73206812dup	NC_000002.12:g.73206811_73206812dup	NC_000002.12:g.73206810_73206812dup	NC_000002.12:g.73206809_73206812dup	NC_000002.12:g.73206808_73206812dup	NC_000002.12:g.73206807_73206812dup	NC_000002.12:g.73206812_73206813insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 2	NC_000002.11:g.73433916_73433940=	NC_000002.11:g.73433929_73433940del	NC_000002.11:g.73433930_73433940del	NC_000002.11:g.73433931_73433940del	NC_000002.11:g.73433932_73433940del	NC_000002.11:g.73433933_73433940del	NC_000002.11:g.73433934_73433940del	NC_000002.11:g.73433935_73433940del	NC_000002.11:g.73433936_73433940del	NC_000002.11:g.73433937_73433940del	NC_000002.11:g.73433938_73433940del	NC_000002.11:g.73433939_73433940del	NC_000002.11:g.73433940del	NC_000002.11:g.73433940dup	NC_000002.11:g.73433939_73433940dup	NC_000002.11:g.73433938_73433940dup	NC_000002.11:g.73433937_73433940dup	NC_000002.11:g.73433936_73433940dup	NC_000002.11:g.73433935_73433940dup	NC_000002.11:g.73433940_73433941insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NOTO transcript	NM_001134462.1:c.383-1612=	NM_001134462.1:c.383-1599_383-1588del	NM_001134462.1:c.383-1598_383-1588del	NM_001134462.1:c.383-1597_383-1588del	NM_001134462.1:c.383-1596_383-1588del	NM_001134462.1:c.383-1595_383-1588del	NM_001134462.1:c.383-1594_383-1588del	NM_001134462.1:c.383-1593_383-1588del	NM_001134462.1:c.383-1592_383-1588del	NM_001134462.1:c.383-1591_383-1588del	NM_001134462.1:c.383-1590_383-1588del	NM_001134462.1:c.383-1589_383-1588del	NM_001134462.1:c.383-1588del	NM_001134462.1:c.383-1588dup	NM_001134462.1:c.383-1589_383-1588dup	NM_001134462.1:c.383-1590_383-1588dup	NM_001134462.1:c.383-1591_383-1588dup	NM_001134462.1:c.383-1592_383-1588dup	NM_001134462.1:c.383-1593_383-1588dup	NM_001134462.1:c.383-1588_383-1587insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NOTO transcript	NM_001134462.2:c.383-1612=	NM_001134462.2:c.383-1599_383-1588del	NM_001134462.2:c.383-1598_383-1588del	NM_001134462.2:c.383-1597_383-1588del	NM_001134462.2:c.383-1596_383-1588del	NM_001134462.2:c.383-1595_383-1588del	NM_001134462.2:c.383-1594_383-1588del	NM_001134462.2:c.383-1593_383-1588del	NM_001134462.2:c.383-1592_383-1588del	NM_001134462.2:c.383-1591_383-1588del	NM_001134462.2:c.383-1590_383-1588del	NM_001134462.2:c.383-1589_383-1588del	NM_001134462.2:c.383-1588del	NM_001134462.2:c.383-1588dup	NM_001134462.2:c.383-1589_383-1588dup	NM_001134462.2:c.383-1590_383-1588dup	NM_001134462.2:c.383-1591_383-1588dup	NM_001134462.2:c.383-1592_383-1588dup	NM_001134462.2:c.383-1593_383-1588dup	NM_001134462.2:c.383-1588_383-1587insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

45 SubSNP, 32 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41632212	Oct 11, 2018 (152)
2	HGSV	ss81807566	Oct 11, 2018 (152)
3	HGSV	ss81978730	Oct 11, 2018 (152)
4	SWEGEN	ss2989741820	Nov 08, 2017 (151)
5	MCHAISSO	ss3065747819	Jan 10, 2018 (151)
6	URBANLAB	ss3647063642	Oct 11, 2018 (152)
7	EVA	ss3827053046	Apr 25, 2020 (154)
8	GNOMAD	ss4043934506	Apr 26, 2021 (155)
9	GNOMAD	ss4043934507	Apr 26, 2021 (155)
10	GNOMAD	ss4043934508	Apr 26, 2021 (155)
11	GNOMAD	ss4043934509	Apr 26, 2021 (155)
12	GNOMAD	ss4043934510	Apr 26, 2021 (155)
13	GNOMAD	ss4043934511	Apr 26, 2021 (155)
14	GNOMAD	ss4043934512	Apr 26, 2021 (155)
15	GNOMAD	ss4043934513	Apr 26, 2021 (155)
16	GNOMAD	ss4043934514	Apr 26, 2021 (155)
17	GNOMAD	ss4043934515	Apr 26, 2021 (155)
18	GNOMAD	ss4043934516	Apr 26, 2021 (155)
19	GNOMAD	ss4043934517	Apr 26, 2021 (155)
20	GNOMAD	ss4043934518	Apr 26, 2021 (155)
21	GNOMAD	ss4043934519	Apr 26, 2021 (155)
22	GNOMAD	ss4043934520	Apr 26, 2021 (155)
23	GNOMAD	ss4043934521	Apr 26, 2021 (155)
24	GNOMAD	ss4043934522	Apr 26, 2021 (155)
25	TOPMED	ss4511016366	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5152034576	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5152034577	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5152034578	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5152034579	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5152034580	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5152034581	Apr 26, 2021 (155)
32	1000G_HIGH_COVERAGE	ss5248574588	Oct 12, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5248574589	Oct 12, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5248574590	Oct 12, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5248574591	Oct 12, 2022 (156)
36	HUGCELL_USP	ss5448730133	Oct 12, 2022 (156)
37	HUGCELL_USP	ss5448730134	Oct 12, 2022 (156)
38	HUGCELL_USP	ss5448730135	Oct 12, 2022 (156)
39	HUGCELL_USP	ss5448730136	Oct 12, 2022 (156)
40	TOMMO_GENOMICS	ss5680852807	Oct 12, 2022 (156)
41	TOMMO_GENOMICS	ss5680852808	Oct 12, 2022 (156)
42	TOMMO_GENOMICS	ss5680852809	Oct 12, 2022 (156)
43	TOMMO_GENOMICS	ss5680852810	Oct 12, 2022 (156)
44	TOMMO_GENOMICS	ss5680852811	Oct 12, 2022 (156)
45	TOMMO_GENOMICS	ss5680852812	Oct 12, 2022 (156)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62509728 (NC_000002.12:73206787::T 21928/84396) Row 62509729 (NC_000002.12:73206787::TT 3653/84334) Row 62509730 (NC_000002.12:73206787::TTT 87/84390)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62509728 (NC_000002.12:73206787::T 21928/84396) Row 62509729 (NC_000002.12:73206787::TT 3653/84334) Row 62509730 (NC_000002.12:73206787::TTT 87/84390)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62509728 (NC_000002.12:73206787::T 21928/84396) Row 62509729 (NC_000002.12:73206787::TT 3653/84334) Row 62509730 (NC_000002.12:73206787::TTT 87/84390)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62509728 (NC_000002.12:73206787::T 21928/84396) Row 62509729 (NC_000002.12:73206787::TT 3653/84334) Row 62509730 (NC_000002.12:73206787::TTT 87/84390)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62509728 (NC_000002.12:73206787::T 21928/84396) Row 62509729 (NC_000002.12:73206787::TT 3653/84334) Row 62509730 (NC_000002.12:73206787::TTT 87/84390)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62509728 (NC_000002.12:73206787::T 21928/84396) Row 62509729 (NC_000002.12:73206787::TT 3653/84334) Row 62509730 (NC_000002.12:73206787::TTT 87/84390)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62509728 (NC_000002.12:73206787::T 21928/84396) Row 62509729 (NC_000002.12:73206787::TT 3653/84334) Row 62509730 (NC_000002.12:73206787::TTT 87/84390)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62509728 (NC_000002.12:73206787::T 21928/84396) Row 62509729 (NC_000002.12:73206787::TT 3653/84334) Row 62509730 (NC_000002.12:73206787::TTT 87/84390)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62509728 (NC_000002.12:73206787::T 21928/84396) Row 62509729 (NC_000002.12:73206787::TT 3653/84334) Row 62509730 (NC_000002.12:73206787::TTT 87/84390)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62509728 (NC_000002.12:73206787::T 21928/84396) Row 62509729 (NC_000002.12:73206787::TT 3653/84334) Row 62509730 (NC_000002.12:73206787::TTT 87/84390)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62509728 (NC_000002.12:73206787::T 21928/84396) Row 62509729 (NC_000002.12:73206787::TT 3653/84334) Row 62509730 (NC_000002.12:73206787::TTT 87/84390)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62509728 (NC_000002.12:73206787::T 21928/84396) Row 62509729 (NC_000002.12:73206787::TT 3653/84334) Row 62509730 (NC_000002.12:73206787::TTT 87/84390)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62509728 (NC_000002.12:73206787::T 21928/84396) Row 62509729 (NC_000002.12:73206787::TT 3653/84334) Row 62509730 (NC_000002.12:73206787::TTT 87/84390)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62509728 (NC_000002.12:73206787::T 21928/84396) Row 62509729 (NC_000002.12:73206787::TT 3653/84334) Row 62509730 (NC_000002.12:73206787::TTT 87/84390)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62509728 (NC_000002.12:73206787::T 21928/84396) Row 62509729 (NC_000002.12:73206787::TT 3653/84334) Row 62509730 (NC_000002.12:73206787::TTT 87/84390)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62509728 (NC_000002.12:73206787::T 21928/84396) Row 62509729 (NC_000002.12:73206787::TT 3653/84334) Row 62509730 (NC_000002.12:73206787::TTT 87/84390)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62509728 (NC_000002.12:73206787::T 21928/84396) Row 62509729 (NC_000002.12:73206787::TT 3653/84334) Row 62509730 (NC_000002.12:73206787::TTT 87/84390)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 62509728 (NC_000002.12:73206787::T 21928/84396) Row 62509729 (NC_000002.12:73206787::TT 3653/84334) Row 62509730 (NC_000002.12:73206787::TTT 87/84390)...	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 10003883 (NC_000002.11:73433915::T 4654/16656) Row 10003884 (NC_000002.11:73433915:T: 230/16656) Row 10003885 (NC_000002.11:73433915::TTT 54/16656)...	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 10003883 (NC_000002.11:73433915::T 4654/16656) Row 10003884 (NC_000002.11:73433915:T: 230/16656) Row 10003885 (NC_000002.11:73433915::TTT 54/16656)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 10003883 (NC_000002.11:73433915::T 4654/16656) Row 10003884 (NC_000002.11:73433915:T: 230/16656) Row 10003885 (NC_000002.11:73433915::TTT 54/16656)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 10003883 (NC_000002.11:73433915::T 4654/16656) Row 10003884 (NC_000002.11:73433915:T: 230/16656) Row 10003885 (NC_000002.11:73433915::TTT 54/16656)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 10003883 (NC_000002.11:73433915::T 4654/16656) Row 10003884 (NC_000002.11:73433915:T: 230/16656) Row 10003885 (NC_000002.11:73433915::TTT 54/16656)...	-	Apr 26, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 10003883 (NC_000002.11:73433915::T 4654/16656) Row 10003884 (NC_000002.11:73433915:T: 230/16656) Row 10003885 (NC_000002.11:73433915::TTT 54/16656)...	-	Apr 26, 2021 (155)
70	14KJPN Submission ignored due to conflicting rows: Row 14689911 (NC_000002.12:73206787::TT 565/26924) Row 14689912 (NC_000002.12:73206787::T 6694/26924) Row 14689913 (NC_000002.12:73206787:T: 347/26924)...	-	Oct 12, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 14689911 (NC_000002.12:73206787::TT 565/26924) Row 14689912 (NC_000002.12:73206787::T 6694/26924) Row 14689913 (NC_000002.12:73206787:T: 347/26924)...	-	Oct 12, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 14689911 (NC_000002.12:73206787::TT 565/26924) Row 14689912 (NC_000002.12:73206787::T 6694/26924) Row 14689913 (NC_000002.12:73206787:T: 347/26924)...	-	Oct 12, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 14689911 (NC_000002.12:73206787::TT 565/26924) Row 14689912 (NC_000002.12:73206787::T 6694/26924) Row 14689913 (NC_000002.12:73206787:T: 347/26924)...	-	Oct 12, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 14689911 (NC_000002.12:73206787::TT 565/26924) Row 14689912 (NC_000002.12:73206787::T 6694/26924) Row 14689913 (NC_000002.12:73206787:T: 347/26924)...	-	Oct 12, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 14689911 (NC_000002.12:73206787::TT 565/26924) Row 14689912 (NC_000002.12:73206787::T 6694/26924) Row 14689913 (NC_000002.12:73206787:T: 347/26924)...	-	Oct 12, 2022 (156)
76	TopMed	NC_000002.12 - 73206788	Apr 26, 2021 (155)
77	ALFA	NC_000002.12 - 73206788	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
314839245, ss4043934522, ss4511016366	NC_000002.12:73206787:TTTTTTTTTTTT:	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
11760082569	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
11760082569	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4043934521	NC_000002.12:73206787:TTTTTTTTTT:	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
11760082569	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4043934520	NC_000002.12:73206787:TTTTTTTTT:	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4043934519	NC_000002.12:73206787:TTTTTTTT:	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
11760082569	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4043934518	NC_000002.12:73206787:TTTTTTT:	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
11760082569	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5152034581	NC_000002.11:73433915:TTTTTT:	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4043934517	NC_000002.12:73206787:TTTTTT:	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
11760082569	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4043934516, ss5248574591	NC_000002.12:73206787:TTTTT:	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
11760082569	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4043934515	NC_000002.12:73206787:TTTT:	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
11760082569	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4043934514	NC_000002.12:73206787:TTT:	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
11760082569	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss2989741820	NC_000002.11:73433915:TT:	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4043934513, ss5248574590, ss5448730136, ss5680852812	NC_000002.12:73206787:TT:	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
11760082569	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5152034577	NC_000002.11:73433915:T:	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5248574588, ss5448730135, ss5680852809	NC_000002.12:73206787:T:	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
11760082569	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3827053046, ss5152034576	NC_000002.11:73433915::T	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3065747819, ss3647063642, ss4043934506, ss5448730133, ss5680852808	NC_000002.12:73206787::T	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11760082569	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss41632212	NT_022184.15:52255827::T	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5152034579	NC_000002.11:73433915::TT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4043934507, ss5248574589, ss5448730134, ss5680852807	NC_000002.12:73206787::TT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11760082569	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss81807566, ss81978730	NT_022184.15:52255827::TT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5152034578	NC_000002.11:73433915::TTT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4043934508, ss5680852810	NC_000002.12:73206787::TTT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11760082569	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5152034580	NC_000002.11:73433915::TTTT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4043934509, ss5680852811	NC_000002.12:73206787::TTTT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11760082569	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4043934510	NC_000002.12:73206787::TTTTT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4043934511	NC_000002.12:73206787::TTTTTT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4043934512	NC_000002.12:73206787::TTTTTTTTTTT… NC_000002.12:73206787::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2397514543	NC_000002.11:73433915:TTTTTTTTTTTT:	NC_000002.12:73206787:TTTTTTTTTTTT… NC_000002.12:73206787:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT

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

No publications for rs969908382

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

rs969908382