Name: rs34967554
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.

rs34967554

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:238318943-238318957 (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)₄ / delTTT / delTT / delT / …
del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₈
Variation Type: Indel Insertion and Deletion
Frequency: dupTTT=0.0791 (744/9406, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TRAF3IP1 : 2KB Upstream 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	9406	TTTTTTTTTTTTTTT=0.8873	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0324, TTTTTTTTTTTTTT=0.0003, TTTTTTTTTTTTTTTT=0.0002, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0791, TTTTTTTTTTTTTTTTTTT=0.0006	0.869891	0.027702	0.102407	32
European	Sub	7622	TTTTTTTTTTTTTTT=0.8612	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0398, TTTTTTTTTTTTTT=0.0004, TTTTTTTTTTTTTTTT=0.0003, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0976, TTTTTTTTTTTTTTTTTTT=0.0008	0.836938	0.034718	0.128344	32
African	Sub	1098	TTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	42	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1056	TTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	82	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	62	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	20	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	68	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	284	TTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	38	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	214	TTTTTTTTTTTTTTT=0.991	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.009, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	9406	(T)₁₅=0.8873	del(T)₄=0.0000, delTTT=0.0000, delTT=0.0324, delT=0.0003, dupT=0.0002, dupTT=0.0000, dupTTT=0.0791, dup(T)₄=0.0006
Allele Frequency Aggregator	European	Sub	7622	(T)₁₅=0.8612	del(T)₄=0.0000, delTTT=0.0000, delTT=0.0398, delT=0.0004, dupT=0.0003, dupTT=0.0000, dupTTT=0.0976, dup(T)₄=0.0008
Allele Frequency Aggregator	African	Sub	1098	(T)₁₅=1.0000	del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	284	(T)₁₅=1.000	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	214	(T)₁₅=0.991	del(T)₄=0.000, delTTT=0.000, delTT=0.009, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Asian	Sub	82	(T)₁₅=1.00	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	Latin American 1	Sub	68	(T)₁₅=1.00	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	38	(T)₁₅=1.00	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.238318954_238318957del
GRCh38.p14 chr 2	NC_000002.12:g.238318955_238318957del
GRCh38.p14 chr 2	NC_000002.12:g.238318956_238318957del
GRCh38.p14 chr 2	NC_000002.12:g.238318957del
GRCh38.p14 chr 2	NC_000002.12:g.238318957dup
GRCh38.p14 chr 2	NC_000002.12:g.238318956_238318957dup
GRCh38.p14 chr 2	NC_000002.12:g.238318955_238318957dup
GRCh38.p14 chr 2	NC_000002.12:g.238318954_238318957dup
GRCh38.p14 chr 2	NC_000002.12:g.238318953_238318957dup
GRCh38.p14 chr 2	NC_000002.12:g.238318952_238318957dup
GRCh38.p14 chr 2	NC_000002.12:g.238318950_238318957dup
GRCh37.p13 chr 2	NC_000002.11:g.239227595_239227598del
GRCh37.p13 chr 2	NC_000002.11:g.239227596_239227598del
GRCh37.p13 chr 2	NC_000002.11:g.239227597_239227598del
GRCh37.p13 chr 2	NC_000002.11:g.239227598del
GRCh37.p13 chr 2	NC_000002.11:g.239227598dup
GRCh37.p13 chr 2	NC_000002.11:g.239227597_239227598dup
GRCh37.p13 chr 2	NC_000002.11:g.239227596_239227598dup
GRCh37.p13 chr 2	NC_000002.11:g.239227595_239227598dup
GRCh37.p13 chr 2	NC_000002.11:g.239227594_239227598dup
GRCh37.p13 chr 2	NC_000002.11:g.239227593_239227598dup
GRCh37.p13 chr 2	NC_000002.11:g.239227591_239227598dup
TRAF3IP1 RefSeqGene	NG_053055.1:g.3466_3469del
TRAF3IP1 RefSeqGene	NG_053055.1:g.3467_3469del
TRAF3IP1 RefSeqGene	NG_053055.1:g.3468_3469del
TRAF3IP1 RefSeqGene	NG_053055.1:g.3469del
TRAF3IP1 RefSeqGene	NG_053055.1:g.3469dup
TRAF3IP1 RefSeqGene	NG_053055.1:g.3468_3469dup
TRAF3IP1 RefSeqGene	NG_053055.1:g.3467_3469dup
TRAF3IP1 RefSeqGene	NG_053055.1:g.3466_3469dup
TRAF3IP1 RefSeqGene	NG_053055.1:g.3465_3469dup
TRAF3IP1 RefSeqGene	NG_053055.1:g.3464_3469dup
TRAF3IP1 RefSeqGene	NG_053055.1:g.3462_3469dup

Gene: TRAF3IP1, TRAF3 interacting protein 1 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
TRAF3IP1 transcript variant 2	NM_001139490.1:c.	N/A	Upstream Transcript Variant
TRAF3IP1 transcript variant 1	NM_015650.4:c.	N/A	Upstream Transcript Variant
TRAF3IP1 transcript variant X6	XM_006712414.3:c.	N/A	Upstream Transcript Variant
TRAF3IP1 transcript variant X1	XM_011510944.3:c.	N/A	Upstream Transcript Variant
TRAF3IP1 transcript variant X3	XM_011510945.3:c.	N/A	Upstream Transcript Variant
TRAF3IP1 transcript variant X4	XM_011510946.3:c.	N/A	Upstream Transcript Variant
TRAF3IP1 transcript variant X5	XM_011510948.3:c.	N/A	Upstream Transcript Variant
TRAF3IP1 transcript variant X2	XM_017003789.2:c.	N/A	Upstream Transcript Variant
TRAF3IP1 transcript variant X7	XM_047443898.1:c.	N/A	Upstream Transcript Variant
TRAF3IP1 transcript variant X9	XM_011510950.3:c.	N/A	N/A
TRAF3IP1 transcript variant X8	XR_922902.3:n.	N/A	Upstream Transcript Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₁₅=	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₈
GRCh38.p14 chr 2	NC_000002.12:g.238318943_238318957=	NC_000002.12:g.238318954_238318957del	NC_000002.12:g.238318955_238318957del	NC_000002.12:g.238318956_238318957del	NC_000002.12:g.238318957del	NC_000002.12:g.238318957dup	NC_000002.12:g.238318956_238318957dup	NC_000002.12:g.238318955_238318957dup	NC_000002.12:g.238318954_238318957dup	NC_000002.12:g.238318953_238318957dup	NC_000002.12:g.238318952_238318957dup	NC_000002.12:g.238318950_238318957dup
GRCh37.p13 chr 2	NC_000002.11:g.239227584_239227598=	NC_000002.11:g.239227595_239227598del	NC_000002.11:g.239227596_239227598del	NC_000002.11:g.239227597_239227598del	NC_000002.11:g.239227598del	NC_000002.11:g.239227598dup	NC_000002.11:g.239227597_239227598dup	NC_000002.11:g.239227596_239227598dup	NC_000002.11:g.239227595_239227598dup	NC_000002.11:g.239227594_239227598dup	NC_000002.11:g.239227593_239227598dup	NC_000002.11:g.239227591_239227598dup
TRAF3IP1 RefSeqGene	NG_053055.1:g.3455_3469=	NG_053055.1:g.3466_3469del	NG_053055.1:g.3467_3469del	NG_053055.1:g.3468_3469del	NG_053055.1:g.3469del	NG_053055.1:g.3469dup	NG_053055.1:g.3468_3469dup	NG_053055.1:g.3467_3469dup	NG_053055.1:g.3466_3469dup	NG_053055.1:g.3465_3469dup	NG_053055.1:g.3464_3469dup	NG_053055.1:g.3462_3469dup

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#.

60 SubSNP, 32 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41642937	Mar 14, 2006 (126)
2	HUMANGENOME_JCVI	ss95307073	Oct 11, 2018 (152)
3	PJP	ss295033609	May 09, 2011 (134)
4	SSMP	ss663295684	Jan 10, 2018 (151)
5	EVA_UK10K_TWINSUK	ss1703467886	Jan 10, 2018 (151)
6	EVA_UK10K_ALSPAC	ss1703467897	Jan 10, 2018 (151)
7	EVA_UK10K_TWINSUK	ss1710061999	Apr 01, 2015 (144)
8	EVA_UK10K_ALSPAC	ss1710062004	Apr 01, 2015 (144)
9	SWEGEN	ss2991617137	Jan 10, 2018 (151)
10	MCHAISSO	ss3064841683	Jan 10, 2018 (151)
11	EVA_DECODE	ss3706339642	Jul 13, 2019 (153)
12	EVA_DECODE	ss3706339643	Jul 13, 2019 (153)
13	EVA_DECODE	ss3706339644	Jul 13, 2019 (153)
14	EVA_DECODE	ss3706339645	Jul 13, 2019 (153)
15	EVA_DECODE	ss3706339646	Jul 13, 2019 (153)
16	EVA_DECODE	ss3706339647	Jul 13, 2019 (153)
17	PACBIO	ss3784197017	Jul 13, 2019 (153)
18	PACBIO	ss3789728975	Jul 13, 2019 (153)
19	PACBIO	ss3794602539	Jul 13, 2019 (153)
20	EVA	ss3827590198	Apr 25, 2020 (154)
21	EVA	ss3842637810	Apr 25, 2020 (154)
22	KOGIC	ss3950411983	Apr 25, 2020 (154)
23	KOGIC	ss3950411984	Apr 25, 2020 (154)
24	KOGIC	ss3950411985	Apr 25, 2020 (154)
25	KOGIC	ss3950411986	Apr 25, 2020 (154)
26	KOGIC	ss3950411987	Apr 25, 2020 (154)
27	KOGIC	ss3950411988	Apr 25, 2020 (154)
28	GNOMAD	ss4063773645	Apr 26, 2021 (155)
29	GNOMAD	ss4063773646	Apr 26, 2021 (155)
30	GNOMAD	ss4063773647	Apr 26, 2021 (155)
31	GNOMAD	ss4063773648	Apr 26, 2021 (155)
32	GNOMAD	ss4063773649	Apr 26, 2021 (155)
33	GNOMAD	ss4063773650	Apr 26, 2021 (155)
34	GNOMAD	ss4063773651	Apr 26, 2021 (155)
35	GNOMAD	ss4063773652	Apr 26, 2021 (155)
36	GNOMAD	ss4063773653	Apr 26, 2021 (155)
37	GNOMAD	ss4063773654	Apr 26, 2021 (155)
38	GNOMAD	ss4063773655	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5157217851	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5157217852	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5157217853	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5157217854	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5157217855	Apr 26, 2021 (155)
44	1000G_HIGH_COVERAGE	ss5252592166	Oct 12, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5252592167	Oct 12, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5252592168	Oct 12, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5252592169	Oct 12, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5252592170	Oct 12, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5252592171	Oct 12, 2022 (156)
50	HUGCELL_USP	ss5452148516	Oct 12, 2022 (156)
51	HUGCELL_USP	ss5452148517	Oct 12, 2022 (156)
52	HUGCELL_USP	ss5452148518	Oct 12, 2022 (156)
53	HUGCELL_USP	ss5452148519	Oct 12, 2022 (156)
54	HUGCELL_USP	ss5452148520	Oct 12, 2022 (156)
55	HUGCELL_USP	ss5452148521	Oct 12, 2022 (156)
56	TOMMO_GENOMICS	ss5688316882	Oct 12, 2022 (156)
57	TOMMO_GENOMICS	ss5688316883	Oct 12, 2022 (156)
58	TOMMO_GENOMICS	ss5688316884	Oct 12, 2022 (156)
59	TOMMO_GENOMICS	ss5688316885	Oct 12, 2022 (156)
60	TOMMO_GENOMICS	ss5688316887	Oct 12, 2022 (156)
61	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 7431896 (NC_000002.11:239227583::TTT 1209/3854) Row 7431897 (NC_000002.11:239227583:TT: 336/3854)	-	Oct 11, 2018 (152)
62	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 7431896 (NC_000002.11:239227583::TTT 1209/3854) Row 7431897 (NC_000002.11:239227583:TT: 336/3854)	-	Oct 11, 2018 (152)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 95455003 (NC_000002.12:238318942::T 1006/127222) Row 95455004 (NC_000002.12:238318942::TT 6899/127190) Row 95455005 (NC_000002.12:238318942::TTT 29375/126976)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 95455003 (NC_000002.12:238318942::T 1006/127222) Row 95455004 (NC_000002.12:238318942::TT 6899/127190) Row 95455005 (NC_000002.12:238318942::TTT 29375/126976)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 95455003 (NC_000002.12:238318942::T 1006/127222) Row 95455004 (NC_000002.12:238318942::TT 6899/127190) Row 95455005 (NC_000002.12:238318942::TTT 29375/126976)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 95455003 (NC_000002.12:238318942::T 1006/127222) Row 95455004 (NC_000002.12:238318942::TT 6899/127190) Row 95455005 (NC_000002.12:238318942::TTT 29375/126976)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 95455003 (NC_000002.12:238318942::T 1006/127222) Row 95455004 (NC_000002.12:238318942::TT 6899/127190) Row 95455005 (NC_000002.12:238318942::TTT 29375/126976)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 95455003 (NC_000002.12:238318942::T 1006/127222) Row 95455004 (NC_000002.12:238318942::TT 6899/127190) Row 95455005 (NC_000002.12:238318942::TTT 29375/126976)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 95455003 (NC_000002.12:238318942::T 1006/127222) Row 95455004 (NC_000002.12:238318942::TT 6899/127190) Row 95455005 (NC_000002.12:238318942::TTT 29375/126976)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 95455003 (NC_000002.12:238318942::T 1006/127222) Row 95455004 (NC_000002.12:238318942::TT 6899/127190) Row 95455005 (NC_000002.12:238318942::TTT 29375/126976)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 95455003 (NC_000002.12:238318942::T 1006/127222) Row 95455004 (NC_000002.12:238318942::TT 6899/127190) Row 95455005 (NC_000002.12:238318942::TTT 29375/126976)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 95455003 (NC_000002.12:238318942::T 1006/127222) Row 95455004 (NC_000002.12:238318942::TT 6899/127190) Row 95455005 (NC_000002.12:238318942::TTT 29375/126976)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 95455003 (NC_000002.12:238318942::T 1006/127222) Row 95455004 (NC_000002.12:238318942::TT 6899/127190) Row 95455005 (NC_000002.12:238318942::TTT 29375/126976)...	-	Apr 26, 2021 (155)
74	Korean Genome Project Submission ignored due to conflicting rows: Row 6789984 (NC_000002.12:238318943:T: 90/1824) Row 6789985 (NC_000002.12:238318944::T 83/1824) Row 6789986 (NC_000002.12:238318944::TTT 121/1824)...	-	Apr 25, 2020 (154)
75	Korean Genome Project Submission ignored due to conflicting rows: Row 6789984 (NC_000002.12:238318943:T: 90/1824) Row 6789985 (NC_000002.12:238318944::T 83/1824) Row 6789986 (NC_000002.12:238318944::TTT 121/1824)...	-	Apr 25, 2020 (154)
76	Korean Genome Project Submission ignored due to conflicting rows: Row 6789984 (NC_000002.12:238318943:T: 90/1824) Row 6789985 (NC_000002.12:238318944::T 83/1824) Row 6789986 (NC_000002.12:238318944::TTT 121/1824)...	-	Apr 25, 2020 (154)
77	Korean Genome Project Submission ignored due to conflicting rows: Row 6789984 (NC_000002.12:238318943:T: 90/1824) Row 6789985 (NC_000002.12:238318944::T 83/1824) Row 6789986 (NC_000002.12:238318944::TTT 121/1824)...	-	Apr 25, 2020 (154)
78	Korean Genome Project Submission ignored due to conflicting rows: Row 6789984 (NC_000002.12:238318943:T: 90/1824) Row 6789985 (NC_000002.12:238318944::T 83/1824) Row 6789986 (NC_000002.12:238318944::TTT 121/1824)...	-	Apr 25, 2020 (154)
79	Korean Genome Project Submission ignored due to conflicting rows: Row 6789984 (NC_000002.12:238318943:T: 90/1824) Row 6789985 (NC_000002.12:238318944::T 83/1824) Row 6789986 (NC_000002.12:238318944::TTT 121/1824)...	-	Apr 25, 2020 (154)
80	8.3KJPN Submission ignored due to conflicting rows: Row 15187158 (NC_000002.11:239227583::TTT 1489/16740) Row 15187159 (NC_000002.11:239227583:T: 15/16740) Row 15187160 (NC_000002.11:239227583::T 15/16740)...	-	Apr 26, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 15187158 (NC_000002.11:239227583::TTT 1489/16740) Row 15187159 (NC_000002.11:239227583:T: 15/16740) Row 15187160 (NC_000002.11:239227583::T 15/16740)...	-	Apr 26, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 15187158 (NC_000002.11:239227583::TTT 1489/16740) Row 15187159 (NC_000002.11:239227583:T: 15/16740) Row 15187160 (NC_000002.11:239227583::T 15/16740)...	-	Apr 26, 2021 (155)
83	8.3KJPN Submission ignored due to conflicting rows: Row 15187158 (NC_000002.11:239227583::TTT 1489/16740) Row 15187159 (NC_000002.11:239227583:T: 15/16740) Row 15187160 (NC_000002.11:239227583::T 15/16740)...	-	Apr 26, 2021 (155)
84	8.3KJPN Submission ignored due to conflicting rows: Row 15187158 (NC_000002.11:239227583::TTT 1489/16740) Row 15187159 (NC_000002.11:239227583:T: 15/16740) Row 15187160 (NC_000002.11:239227583::T 15/16740)...	-	Apr 26, 2021 (155)
85	14KJPN Submission ignored due to conflicting rows: Row 22153986 (NC_000002.12:238318942::TTT 2691/28254) Row 22153987 (NC_000002.12:238318942:TT: 499/28254) Row 22153988 (NC_000002.12:238318942::T 11/28254)...	-	Oct 12, 2022 (156)
86	14KJPN Submission ignored due to conflicting rows: Row 22153986 (NC_000002.12:238318942::TTT 2691/28254) Row 22153987 (NC_000002.12:238318942:TT: 499/28254) Row 22153988 (NC_000002.12:238318942::T 11/28254)...	-	Oct 12, 2022 (156)
87	14KJPN Submission ignored due to conflicting rows: Row 22153986 (NC_000002.12:238318942::TTT 2691/28254) Row 22153987 (NC_000002.12:238318942:TT: 499/28254) Row 22153988 (NC_000002.12:238318942::T 11/28254)...	-	Oct 12, 2022 (156)
88	14KJPN Submission ignored due to conflicting rows: Row 22153986 (NC_000002.12:238318942::TTT 2691/28254) Row 22153987 (NC_000002.12:238318942:TT: 499/28254) Row 22153988 (NC_000002.12:238318942::T 11/28254)...	-	Oct 12, 2022 (156)
89	14KJPN Submission ignored due to conflicting rows: Row 22153986 (NC_000002.12:238318942::TTT 2691/28254) Row 22153987 (NC_000002.12:238318942:TT: 499/28254) Row 22153988 (NC_000002.12:238318942::T 11/28254)...	-	Oct 12, 2022 (156)
90	UK 10K study - Twins Submission ignored due to conflicting rows: Row 7431896 (NC_000002.11:239227583::TTT 1172/3708) Row 7431897 (NC_000002.11:239227583:TT: 346/3708)	-	Oct 11, 2018 (152)
91	UK 10K study - Twins Submission ignored due to conflicting rows: Row 7431896 (NC_000002.11:239227583::TTT 1172/3708) Row 7431897 (NC_000002.11:239227583:TT: 346/3708)	-	Oct 11, 2018 (152)
92	ALFA	NC_000002.12 - 238318943	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)
rs371323024	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4063773655	NC_000002.12:238318942:TTTT:	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
12424732668	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4063773654	NC_000002.12:238318942:TTT:	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
12424732668	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss663295684, ss1703467886, ss1703467897, ss2991617137, ss3827590198, ss5157217854	NC_000002.11:239227583:TT:	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3064841683, ss3706339642, ss3950411986, ss4063773653, ss5252592166, ss5452148519, ss5688316883	NC_000002.12:238318942:TT:	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
12424732668	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss5157217852	NC_000002.11:239227583:T:	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4063773652, ss5252592170, ss5452148518, ss5688316885	NC_000002.12:238318942:T:	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
12424732668	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3706339643, ss3950411983	NC_000002.12:238318943:T:	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss5157217853	NC_000002.11:239227583::T	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4063773645, ss5252592167, ss5452148521, ss5688316884	NC_000002.12:238318942::T	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
12424732668	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3706339644, ss3950411984	NC_000002.12:238318944::T	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4063773646, ss5252592169, ss5452148520	NC_000002.12:238318942::TT	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
12424732668	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3706339645, ss3950411987	NC_000002.12:238318944::TT	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss295033609	NC_000002.10:238892335::TTT	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3784197017, ss3789728975, ss3794602539, ss5157217851	NC_000002.11:239227583::TTT	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss1710061999, ss1710062004	NC_000002.11:239227585::TTT	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3842637810, ss4063773647, ss5252592168, ss5452148516, ss5688316882	NC_000002.12:238318942::TTT	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
12424732668	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3706339646, ss3950411985	NC_000002.12:238318944::TTT	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss41642937	NT_005120.16:5173842::TTT	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss95307073	NT_005120.16:5173857::TTT	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5157217855	NC_000002.11:239227583::TTTT	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4063773648, ss5252592171, ss5452148517, ss5688316887	NC_000002.12:238318942::TTTT	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
12424732668	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3706339647, ss3950411988	NC_000002.12:238318944::TTTT	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4063773649	NC_000002.12:238318942::TTTTT	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4063773650	NC_000002.12:238318942::TTTTTT	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4063773651	NC_000002.12:238318942::TTTTTTTT	NC_000002.12:238318942:TTTTTTTTTTT… NC_000002.12:238318942:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(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 rs34967554

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

rs34967554