Name: rs34070901
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.

rs34070901

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:121726519-121726535 (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)₉ / del(T)₇ / del(T)₆ / del(…
del(T)₉ / 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)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: (T)₁₇=0.4429 (2218/5008, 1000G)
(T)₁₇=0.3604 (1681/4664, ALFA)
(T)₁₇=0.0184 (71/3854, ALSPAC) (+ 1 more)
(T)₁₇=0.0232 (86/3708, TWINSUK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NIFK-AS1 : Intron Variant
NIFK : 500B Downstream 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	4664	TTTTTTTTTTTTTTTTT=0.3604	TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0084, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0071, TTTTTTTTTTTTTTTTTT=0.6126, TTTTTTTTTTTTTTTTTTT=0.0116, TTTTTTTTTTTTTTTTTTTT=0.0000	0.304917	0.559765	0.135318	32
European	Sub	4576	TTTTTTTTTTTTTTTTT=0.3492	TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0085, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0070, TTTTTTTTTTTTTTTTTT=0.6235, TTTTTTTTTTTTTTTTTTT=0.0118, TTTTTTTTTTTTTTTTTTTT=0.0000	0.292088	0.569917	0.137994	32
African	Sub	58	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African Others	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
African American	Sub	58	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Asian	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
East Asian	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTT=0	TTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	4	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	4	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	4	TTTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other	Sub	18	TTTTTTTTTTTTTTTTT=0.72	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.06, TTTTTTTTTTTTTTTTTT=0.22, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	0.75	0.25	0.0	5

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
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupT=0.5571
1000Genomes	African	Sub	1322	- No frequency provided	dupT=0.3548
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupT=0.6825
1000Genomes	Europe	Sub	1006	- No frequency provided	dupT=0.6372
1000Genomes	South Asian	Sub	978	- No frequency provided	dupT=0.589
1000Genomes	American	Sub	694	- No frequency provided	dupT=0.599
Allele Frequency Aggregator	Total	Global	4664	(T)₁₇=0.3604	del(T)₉=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0084, delTTT=0.0000, delTT=0.0000, delT=0.0071, dupT=0.6126, dupTT=0.0116, dupTTT=0.0000
Allele Frequency Aggregator	European	Sub	4576	(T)₁₇=0.3492	del(T)₉=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0085, delTTT=0.0000, delTT=0.0000, delT=0.0070, dupT=0.6235, dupTT=0.0118, dupTTT=0.0000
Allele Frequency Aggregator	African	Sub	58	(T)₁₇=1.00	del(T)₉=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
Allele Frequency Aggregator	Other	Sub	18	(T)₁₇=0.72	del(T)₉=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=0.06, dupT=0.22, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Latin American 1	Sub	4	(T)₁₇=1.0	del(T)₉=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
Allele Frequency Aggregator	Latin American 2	Sub	4	(T)₁₇=1.0	del(T)₉=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
Allele Frequency Aggregator	South Asian	Sub	4	(T)₁₇=1.0	del(T)₉=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
Allele Frequency Aggregator	Asian	Sub	0	(T)₁₇=0	del(T)₉=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
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	- No frequency provided	dupT=0.9816
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	- No frequency provided	dupT=0.9768

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.121726527_121726535del
GRCh38.p14 chr 2	NC_000002.12:g.121726529_121726535del
GRCh38.p14 chr 2	NC_000002.12:g.121726530_121726535del
GRCh38.p14 chr 2	NC_000002.12:g.121726531_121726535del
GRCh38.p14 chr 2	NC_000002.12:g.121726532_121726535del
GRCh38.p14 chr 2	NC_000002.12:g.121726533_121726535del
GRCh38.p14 chr 2	NC_000002.12:g.121726534_121726535del
GRCh38.p14 chr 2	NC_000002.12:g.121726535del
GRCh38.p14 chr 2	NC_000002.12:g.121726535dup
GRCh38.p14 chr 2	NC_000002.12:g.121726534_121726535dup
GRCh38.p14 chr 2	NC_000002.12:g.121726533_121726535dup
GRCh38.p14 chr 2	NC_000002.12:g.121726532_121726535dup
GRCh38.p14 chr 2	NC_000002.12:g.121726531_121726535dup
GRCh38.p14 chr 2	NC_000002.12:g.121726526_121726535dup
GRCh37.p13 chr 2	NC_000002.11:g.122484103_122484111del
GRCh37.p13 chr 2	NC_000002.11:g.122484105_122484111del
GRCh37.p13 chr 2	NC_000002.11:g.122484106_122484111del
GRCh37.p13 chr 2	NC_000002.11:g.122484107_122484111del
GRCh37.p13 chr 2	NC_000002.11:g.122484108_122484111del
GRCh37.p13 chr 2	NC_000002.11:g.122484109_122484111del
GRCh37.p13 chr 2	NC_000002.11:g.122484110_122484111del
GRCh37.p13 chr 2	NC_000002.11:g.122484111del
GRCh37.p13 chr 2	NC_000002.11:g.122484111dup
GRCh37.p13 chr 2	NC_000002.11:g.122484110_122484111dup
GRCh37.p13 chr 2	NC_000002.11:g.122484109_122484111dup
GRCh37.p13 chr 2	NC_000002.11:g.122484108_122484111dup
GRCh37.p13 chr 2	NC_000002.11:g.122484107_122484111dup
GRCh37.p13 chr 2	NC_000002.11:g.122484102_122484111dup

Gene: NIFK, nucleolar protein interacting with the FHA domain of MKI67 (minus strand) : 500B Downstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
NIFK transcript	NM_032390.5:c.	N/A	Downstream Transcript Variant

Gene: NIFK-AS1, NIFK antisense RNA 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NIFK-AS1 transcript variant 3	NR_037857.1:n.	N/A	Intron Variant
NIFK-AS1 transcript variant 1	NR_037856.1:n.	N/A	Genic Downstream Transcript Variant
NIFK-AS1 transcript variant 2	NR_037858.1:n.	N/A	Genic Downstream 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)₁₇=	del(T)₉	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)₁₀
GRCh38.p14 chr 2	NC_000002.12:g.121726519_121726535=	NC_000002.12:g.121726527_121726535del	NC_000002.12:g.121726529_121726535del	NC_000002.12:g.121726530_121726535del	NC_000002.12:g.121726531_121726535del	NC_000002.12:g.121726532_121726535del	NC_000002.12:g.121726533_121726535del	NC_000002.12:g.121726534_121726535del	NC_000002.12:g.121726535del	NC_000002.12:g.121726535dup	NC_000002.12:g.121726534_121726535dup	NC_000002.12:g.121726533_121726535dup	NC_000002.12:g.121726532_121726535dup	NC_000002.12:g.121726531_121726535dup	NC_000002.12:g.121726526_121726535dup
GRCh37.p13 chr 2	NC_000002.11:g.122484095_122484111=	NC_000002.11:g.122484103_122484111del	NC_000002.11:g.122484105_122484111del	NC_000002.11:g.122484106_122484111del	NC_000002.11:g.122484107_122484111del	NC_000002.11:g.122484108_122484111del	NC_000002.11:g.122484109_122484111del	NC_000002.11:g.122484110_122484111del	NC_000002.11:g.122484111del	NC_000002.11:g.122484111dup	NC_000002.11:g.122484110_122484111dup	NC_000002.11:g.122484109_122484111dup	NC_000002.11:g.122484108_122484111dup	NC_000002.11:g.122484107_122484111dup	NC_000002.11:g.122484102_122484111dup

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#.

55 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41698373	Mar 13, 2006 (126)
2	ABI	ss41797360	Mar 14, 2006 (126)
3	HGSV	ss81611296	Dec 03, 2013 (144)
4	HGSV	ss81731924	Dec 15, 2007 (129)
5	HUMANGENOME_JCVI	ss95283314	Dec 05, 2013 (144)
6	PJP	ss295000353	May 09, 2011 (135)
7	PJP	ss295000354	Jan 10, 2018 (151)
8	1000GENOMES	ss1368697179	Aug 21, 2014 (142)
9	DDI	ss1536304210	Apr 01, 2015 (144)
10	EVA_UK10K_ALSPAC	ss1703072809	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1703072810	Apr 01, 2015 (144)
12	HAMMER_LAB	ss1797401862	Sep 08, 2015 (146)
13	SWEGEN	ss2990302705	Nov 08, 2017 (151)
14	MCHAISSO	ss3063953425	Nov 08, 2017 (151)
15	MCHAISSO	ss3064805882	Nov 08, 2017 (151)
16	MCHAISSO	ss3065762969	Nov 08, 2017 (151)
17	EVA_DECODE	ss3704764768	Jul 13, 2019 (153)
18	EVA_DECODE	ss3704764769	Jul 13, 2019 (153)
19	EVA_DECODE	ss3704764770	Jul 13, 2019 (153)
20	EVA_DECODE	ss3704764771	Jul 13, 2019 (153)
21	EVA_DECODE	ss3704764772	Jul 13, 2019 (153)
22	KHV_HUMAN_GENOMES	ss3801665182	Jul 13, 2019 (153)
23	EVA	ss3827187170	Apr 25, 2020 (154)
24	GNOMAD	ss4049589726	Apr 27, 2021 (155)
25	GNOMAD	ss4049589727	Apr 27, 2021 (155)
26	GNOMAD	ss4049589728	Apr 27, 2021 (155)
27	GNOMAD	ss4049589729	Apr 27, 2021 (155)
28	GNOMAD	ss4049589730	Apr 27, 2021 (155)
29	GNOMAD	ss4049589732	Apr 27, 2021 (155)
30	GNOMAD	ss4049589733	Apr 27, 2021 (155)
31	GNOMAD	ss4049589734	Apr 27, 2021 (155)
32	GNOMAD	ss4049589735	Apr 27, 2021 (155)
33	GNOMAD	ss4049589736	Apr 27, 2021 (155)
34	TOMMO_GENOMICS	ss5153545731	Apr 27, 2021 (155)
35	TOMMO_GENOMICS	ss5153545732	Apr 27, 2021 (155)
36	TOMMO_GENOMICS	ss5153545733	Apr 27, 2021 (155)
37	1000G_HIGH_COVERAGE	ss5249764334	Oct 12, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5249764335	Oct 12, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5249764336	Oct 12, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5249764337	Oct 12, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5249764338	Oct 12, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5249764339	Oct 12, 2022 (156)
43	HUGCELL_USP	ss5449627157	Oct 12, 2022 (156)
44	HUGCELL_USP	ss5449627158	Oct 12, 2022 (156)
45	HUGCELL_USP	ss5449627159	Oct 12, 2022 (156)
46	HUGCELL_USP	ss5449627160	Oct 12, 2022 (156)
47	TOMMO_GENOMICS	ss5683574043	Oct 12, 2022 (156)
48	TOMMO_GENOMICS	ss5683574044	Oct 12, 2022 (156)
49	TOMMO_GENOMICS	ss5683574045	Oct 12, 2022 (156)
50	TOMMO_GENOMICS	ss5683574046	Oct 12, 2022 (156)
51	EVA	ss5820708097	Oct 12, 2022 (156)
52	EVA	ss5820708098	Oct 12, 2022 (156)
53	EVA	ss5820708099	Oct 12, 2022 (156)
54	EVA	ss5932111905	Oct 12, 2022 (156)
55	EVA	ss5955873563	Oct 12, 2022 (156)
56	1000Genomes	NC_000002.11 - 122484095	Oct 11, 2018 (152)
57	The Avon Longitudinal Study of Parents and Children	NC_000002.11 - 122484095	Oct 11, 2018 (152)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 71809201 (NC_000002.12:121726518::T 83350/118724) Row 71809202 (NC_000002.12:121726518::TT 1807/118768) Row 71809203 (NC_000002.12:121726518::TTT 9/118808)...	-	Apr 27, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 71809201 (NC_000002.12:121726518::T 83350/118724) Row 71809202 (NC_000002.12:121726518::TT 1807/118768) Row 71809203 (NC_000002.12:121726518::TTT 9/118808)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 71809201 (NC_000002.12:121726518::T 83350/118724) Row 71809202 (NC_000002.12:121726518::TT 1807/118768) Row 71809203 (NC_000002.12:121726518::TTT 9/118808)...	-	Apr 27, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 71809201 (NC_000002.12:121726518::T 83350/118724) Row 71809202 (NC_000002.12:121726518::TT 1807/118768) Row 71809203 (NC_000002.12:121726518::TTT 9/118808)...	-	Apr 27, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 71809201 (NC_000002.12:121726518::T 83350/118724) Row 71809202 (NC_000002.12:121726518::TT 1807/118768) Row 71809203 (NC_000002.12:121726518::TTT 9/118808)...	-	Apr 27, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 71809201 (NC_000002.12:121726518::T 83350/118724) Row 71809202 (NC_000002.12:121726518::TT 1807/118768) Row 71809203 (NC_000002.12:121726518::TTT 9/118808)...	-	Apr 27, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 71809201 (NC_000002.12:121726518::T 83350/118724) Row 71809202 (NC_000002.12:121726518::TT 1807/118768) Row 71809203 (NC_000002.12:121726518::TTT 9/118808)...	-	Apr 27, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 71809201 (NC_000002.12:121726518::T 83350/118724) Row 71809202 (NC_000002.12:121726518::TT 1807/118768) Row 71809203 (NC_000002.12:121726518::TTT 9/118808)...	-	Apr 27, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 71809201 (NC_000002.12:121726518::T 83350/118724) Row 71809202 (NC_000002.12:121726518::TT 1807/118768) Row 71809203 (NC_000002.12:121726518::TTT 9/118808)...	-	Apr 27, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 71809201 (NC_000002.12:121726518::T 83350/118724) Row 71809202 (NC_000002.12:121726518::TT 1807/118768) Row 71809203 (NC_000002.12:121726518::TTT 9/118808)...	-	Apr 27, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 71809201 (NC_000002.12:121726518::T 83350/118724) Row 71809202 (NC_000002.12:121726518::TT 1807/118768) Row 71809203 (NC_000002.12:121726518::TTT 9/118808)...	-	Apr 27, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 11515038 (NC_000002.11:122484094:T: 2676/16218) Row 11515039 (NC_000002.11:122484094::T 10764/16218) Row 11515040 (NC_000002.11:122484094::TT 187/16218)	-	Apr 27, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 11515038 (NC_000002.11:122484094:T: 2676/16218) Row 11515039 (NC_000002.11:122484094::T 10764/16218) Row 11515040 (NC_000002.11:122484094::TT 187/16218)	-	Apr 27, 2021 (155)
71	8.3KJPN Submission ignored due to conflicting rows: Row 11515038 (NC_000002.11:122484094:T: 2676/16218) Row 11515039 (NC_000002.11:122484094::T 10764/16218) Row 11515040 (NC_000002.11:122484094::TT 187/16218)	-	Apr 27, 2021 (155)
72	14KJPN Submission ignored due to conflicting rows: Row 17411147 (NC_000002.12:121726518::T 19015/28254) Row 17411148 (NC_000002.12:121726518:T: 4712/28254) Row 17411149 (NC_000002.12:121726518::TT 353/28254)...	-	Oct 12, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 17411147 (NC_000002.12:121726518::T 19015/28254) Row 17411148 (NC_000002.12:121726518:T: 4712/28254) Row 17411149 (NC_000002.12:121726518::TT 353/28254)...	-	Oct 12, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 17411147 (NC_000002.12:121726518::T 19015/28254) Row 17411148 (NC_000002.12:121726518:T: 4712/28254) Row 17411149 (NC_000002.12:121726518::TT 353/28254)...	-	Oct 12, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 17411147 (NC_000002.12:121726518::T 19015/28254) Row 17411148 (NC_000002.12:121726518:T: 4712/28254) Row 17411149 (NC_000002.12:121726518::TT 353/28254)...	-	Oct 12, 2022 (156)
76	UK 10K study - Twins	NC_000002.11 - 122484095	Oct 11, 2018 (152)
77	ALFA	NC_000002.12 - 121726519	Apr 27, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs397714310	Jul 01, 2015 (144)
rs59654377	May 11, 2012 (137)
rs148150270	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4049589736	NC_000002.12:121726518:TTTTTTTTT:	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
405782658	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTT	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTT	(self)
405782658	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss5249764339	NC_000002.12:121726518:TTTTTT:	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
405782658	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4049589735	NC_000002.12:121726518:TTTTT:	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
405782658	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss2990302705	NC_000002.11:122484094:TTTT:	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3704764768, ss4049589734, ss5249764337, ss5449627159	NC_000002.12:121726518:TTTT:	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
405782658	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4049589733	NC_000002.12:121726518:TTT:	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
405782658	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4049589732, ss5249764338, ss5683574046	NC_000002.12:121726518:TT:	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
405782658	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss81731924	NC_000002.9:122200340:T:	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss1797401862, ss5153545731	NC_000002.11:122484094:T:	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss5249764335, ss5449627158, ss5683574044	NC_000002.12:121726518:T:	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
405782658	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3704764769	NC_000002.12:121726521:T:	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss295000353	NC_000002.10:122200565::T	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss295000354	NC_000002.10:122200581::T	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
10057079, 5553825, 5553825, ss1368697179, ss1536304210, ss1703072809, ss1703072810, ss3827187170, ss5153545732, ss5820708097, ss5955873563	NC_000002.11:122484094::T	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3063953425, ss3064805882, ss3065762969, ss3801665182, ss4049589726, ss5249764334, ss5449627157, ss5683574043, ss5932111905	NC_000002.12:121726518::T	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
405782658	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3704764770	NC_000002.12:121726522::T	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss41698373	NT_022135.16:12232757::T	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss41797360	NT_022135.16:12232758::T	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss81611296, ss95283314	NT_022135.16:12232774::T	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5153545733, ss5820708098	NC_000002.11:122484094::TT	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4049589727, ss5249764336, ss5449627160, ss5683574045	NC_000002.12:121726518::TT	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
405782658	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3704764771	NC_000002.12:121726522::TT	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5820708099	NC_000002.11:122484094::TTT	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT
ss4049589728	NC_000002.12:121726518::TTT	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
405782658	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4049589729	NC_000002.12:121726518::TTTT	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4049589730	NC_000002.12:121726518::TTTTT	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3704764772	NC_000002.12:121726522::TTTTTTTTTT	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3321183914	NC_000002.12:121726518:TTTTTTT:	NC_000002.12:121726518:TTTTTTTTTTT… NC_000002.12:121726518:TTTTTTTTTTTTTTTTT:TTTTTTTTTT

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

No publications for rs34070901

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

rs34070901