Name: rs34111911
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.

rs34111911

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr9:96778528-96778544 (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)₅ / del(T)₄ / delTTT / delTT…
del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₇ / dup(T)₈ / dup(T)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.00872 (113/12964, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZNF510 : 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	12964	TTTTTTTTTTTTTTTTT=0.98774	TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00015, TTTTTTTTTTTTTTTTTT=0.00872, TTTTTTTTTTTTTTTTTTT=0.00339, TTTTTTTTTTTTTTTTTTTT=0.00000	0.983691	0.001243	0.015067	32
European	Sub	11416	TTTTTTTTTTTTTTTTT=0.98607	TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00018, TTTTTTTTTTTTTTTTTT=0.00990, TTTTTTTTTTTTTTTTTTT=0.00385, TTTTTTTTTTTTTTTTTTTT=0.00000	0.981462	0.001412	0.017126	32
African	Sub	500	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	10	TTTTTTTTTTTTTTTTT=1.0	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
African American	Sub	490	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	46	TTTTTTTTTTTTTTTTT=1.00	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
East Asian	Sub	38	TTTTTTTTTTTTTTTTT=1.00	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
Other Asian	Sub	8	TTTTTTTTTTTTTTTTT=1.0	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 1	Sub	98	TTTTTTTTTTTTTTTTT=1.00	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
Latin American 2	Sub	542	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	64	TTTTTTTTTTTTTTTTT=1.00	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
Other	Sub	298	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=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	12964	(T)₁₇=0.98774	del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00015, dupT=0.00872, dupTT=0.00339, dupTTT=0.00000
Allele Frequency Aggregator	European	Sub	11416	(T)₁₇=0.98607	del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00018, dupT=0.00990, dupTT=0.00385, dupTTT=0.00000
Allele Frequency Aggregator	Latin American 2	Sub	542	(T)₁₇=1.000	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
Allele Frequency Aggregator	African	Sub	500	(T)₁₇=1.000	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
Allele Frequency Aggregator	Other	Sub	298	(T)₁₇=1.000	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
Allele Frequency Aggregator	Latin American 1	Sub	98	(T)₁₇=1.00	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	South Asian	Sub	64	(T)₁₇=1.00	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	Asian	Sub	46	(T)₁₇=1.00	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

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 9	NC_000009.12:g.96778540_96778544del
GRCh38.p14 chr 9	NC_000009.12:g.96778541_96778544del
GRCh38.p14 chr 9	NC_000009.12:g.96778542_96778544del
GRCh38.p14 chr 9	NC_000009.12:g.96778543_96778544del
GRCh38.p14 chr 9	NC_000009.12:g.96778544del
GRCh38.p14 chr 9	NC_000009.12:g.96778544dup
GRCh38.p14 chr 9	NC_000009.12:g.96778543_96778544dup
GRCh38.p14 chr 9	NC_000009.12:g.96778542_96778544dup
GRCh38.p14 chr 9	NC_000009.12:g.96778541_96778544dup
GRCh38.p14 chr 9	NC_000009.12:g.96778540_96778544dup
GRCh38.p14 chr 9	NC_000009.12:g.96778538_96778544dup
GRCh38.p14 chr 9	NC_000009.12:g.96778537_96778544dup
GRCh38.p14 chr 9	NC_000009.12:g.96778535_96778544dup
GRCh37.p13 chr 9	NC_000009.11:g.99540822_99540826del
GRCh37.p13 chr 9	NC_000009.11:g.99540823_99540826del
GRCh37.p13 chr 9	NC_000009.11:g.99540824_99540826del
GRCh37.p13 chr 9	NC_000009.11:g.99540825_99540826del
GRCh37.p13 chr 9	NC_000009.11:g.99540826del
GRCh37.p13 chr 9	NC_000009.11:g.99540826dup
GRCh37.p13 chr 9	NC_000009.11:g.99540825_99540826dup
GRCh37.p13 chr 9	NC_000009.11:g.99540824_99540826dup
GRCh37.p13 chr 9	NC_000009.11:g.99540823_99540826dup
GRCh37.p13 chr 9	NC_000009.11:g.99540822_99540826dup
GRCh37.p13 chr 9	NC_000009.11:g.99540820_99540826dup
GRCh37.p13 chr 9	NC_000009.11:g.99540819_99540826dup
GRCh37.p13 chr 9	NC_000009.11:g.99540817_99540826dup

Gene: ZNF510, zinc finger protein 510 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF510 transcript variant 1	NM_001314059.2:c.	N/A	Upstream Transcript Variant
ZNF510 transcript variant 3	NM_001314060.2:c.	N/A	Upstream Transcript Variant
ZNF510 transcript variant 2	NM_014930.3:c.	N/A	Upstream Transcript Variant
ZNF510 transcript variant X2	XM_005251808.3:c.	N/A	Upstream Transcript Variant
ZNF510 transcript variant X1	XM_017014483.2:c.	N/A	Upstream Transcript Variant
ZNF510 transcript variant X3	XM_047423005.1:c.	N/A	Upstream Transcript Variant
ZNF510 transcript variant X4	XM_011518393.3:c.	N/A	N/A

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)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₇	dup(T)₈	dup(T)₁₀
GRCh38.p14 chr 9	NC_000009.12:g.96778528_96778544=	NC_000009.12:g.96778540_96778544del	NC_000009.12:g.96778541_96778544del	NC_000009.12:g.96778542_96778544del	NC_000009.12:g.96778543_96778544del	NC_000009.12:g.96778544del	NC_000009.12:g.96778544dup	NC_000009.12:g.96778543_96778544dup	NC_000009.12:g.96778542_96778544dup	NC_000009.12:g.96778541_96778544dup	NC_000009.12:g.96778540_96778544dup	NC_000009.12:g.96778538_96778544dup	NC_000009.12:g.96778537_96778544dup	NC_000009.12:g.96778535_96778544dup
GRCh37.p13 chr 9	NC_000009.11:g.99540810_99540826=	NC_000009.11:g.99540822_99540826del	NC_000009.11:g.99540823_99540826del	NC_000009.11:g.99540824_99540826del	NC_000009.11:g.99540825_99540826del	NC_000009.11:g.99540826del	NC_000009.11:g.99540826dup	NC_000009.11:g.99540825_99540826dup	NC_000009.11:g.99540824_99540826dup	NC_000009.11:g.99540823_99540826dup	NC_000009.11:g.99540822_99540826dup	NC_000009.11:g.99540820_99540826dup	NC_000009.11:g.99540819_99540826dup	NC_000009.11:g.99540817_99540826dup

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#.

46 SubSNP, 30 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss43434331	Mar 13, 2006 (126)
2	HUMANGENOME_JCVI	ss95521872	Oct 12, 2018 (152)
3	PJP	ss295429999	May 09, 2011 (137)
4	PJP	ss295430000	May 09, 2011 (135)
5	SSMP	ss663945095	Jan 10, 2018 (151)
6	SWEGEN	ss3005282254	Nov 08, 2017 (151)
7	PACBIO	ss3786472842	Jul 13, 2019 (153)
8	EVA	ss3831761542	Apr 26, 2020 (154)
9	KOGIC	ss3966369485	Apr 26, 2020 (154)
10	KOGIC	ss3966369486	Apr 26, 2020 (154)
11	KOGIC	ss3966369487	Apr 26, 2020 (154)
12	KOGIC	ss3966369488	Apr 26, 2020 (154)
13	KOGIC	ss3966369489	Apr 26, 2020 (154)
14	GNOMAD	ss4206168135	Apr 26, 2021 (155)
15	GNOMAD	ss4206168136	Apr 26, 2021 (155)
16	GNOMAD	ss4206168137	Apr 26, 2021 (155)
17	GNOMAD	ss4206168138	Apr 26, 2021 (155)
18	GNOMAD	ss4206168139	Apr 26, 2021 (155)
19	GNOMAD	ss4206168140	Apr 26, 2021 (155)
20	GNOMAD	ss4206168141	Apr 26, 2021 (155)
21	GNOMAD	ss4206168142	Apr 26, 2021 (155)
22	GNOMAD	ss4206168144	Apr 26, 2021 (155)
23	GNOMAD	ss4206168145	Apr 26, 2021 (155)
24	GNOMAD	ss4206168146	Apr 26, 2021 (155)
25	GNOMAD	ss4206168147	Apr 26, 2021 (155)
26	GNOMAD	ss4206168148	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5194441373	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5194441374	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5194441375	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5194441376	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5194441377	Apr 26, 2021 (155)
32	1000G_HIGH_COVERAGE	ss5281517463	Oct 13, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5281517464	Oct 13, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5281517465	Oct 13, 2022 (156)
35	HUGCELL_USP	ss5477450752	Oct 13, 2022 (156)
36	HUGCELL_USP	ss5477450753	Oct 13, 2022 (156)
37	HUGCELL_USP	ss5477450754	Oct 13, 2022 (156)
38	HUGCELL_USP	ss5477450755	Oct 13, 2022 (156)
39	HUGCELL_USP	ss5477450756	Oct 13, 2022 (156)
40	TOMMO_GENOMICS	ss5738721354	Oct 13, 2022 (156)
41	TOMMO_GENOMICS	ss5738721355	Oct 13, 2022 (156)
42	TOMMO_GENOMICS	ss5738721356	Oct 13, 2022 (156)
43	TOMMO_GENOMICS	ss5738721357	Oct 13, 2022 (156)
44	TOMMO_GENOMICS	ss5738721358	Oct 13, 2022 (156)
45	TOMMO_GENOMICS	ss5738721359	Oct 13, 2022 (156)
46	EVA	ss5856854596	Oct 13, 2022 (156)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 332185708 (NC_000009.12:96778527::T 17504/120780) Row 332185709 (NC_000009.12:96778527::TT 6762/120800) Row 332185710 (NC_000009.12:96778527::TTT 208/120840)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 332185708 (NC_000009.12:96778527::T 17504/120780) Row 332185709 (NC_000009.12:96778527::TT 6762/120800) Row 332185710 (NC_000009.12:96778527::TTT 208/120840)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 332185708 (NC_000009.12:96778527::T 17504/120780) Row 332185709 (NC_000009.12:96778527::TT 6762/120800) Row 332185710 (NC_000009.12:96778527::TTT 208/120840)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 332185708 (NC_000009.12:96778527::T 17504/120780) Row 332185709 (NC_000009.12:96778527::TT 6762/120800) Row 332185710 (NC_000009.12:96778527::TTT 208/120840)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 332185708 (NC_000009.12:96778527::T 17504/120780) Row 332185709 (NC_000009.12:96778527::TT 6762/120800) Row 332185710 (NC_000009.12:96778527::TTT 208/120840)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 332185708 (NC_000009.12:96778527::T 17504/120780) Row 332185709 (NC_000009.12:96778527::TT 6762/120800) Row 332185710 (NC_000009.12:96778527::TTT 208/120840)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 332185708 (NC_000009.12:96778527::T 17504/120780) Row 332185709 (NC_000009.12:96778527::TT 6762/120800) Row 332185710 (NC_000009.12:96778527::TTT 208/120840)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 332185708 (NC_000009.12:96778527::T 17504/120780) Row 332185709 (NC_000009.12:96778527::TT 6762/120800) Row 332185710 (NC_000009.12:96778527::TTT 208/120840)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 332185708 (NC_000009.12:96778527::T 17504/120780) Row 332185709 (NC_000009.12:96778527::TT 6762/120800) Row 332185710 (NC_000009.12:96778527::TTT 208/120840)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 332185708 (NC_000009.12:96778527::T 17504/120780) Row 332185709 (NC_000009.12:96778527::TT 6762/120800) Row 332185710 (NC_000009.12:96778527::TTT 208/120840)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 332185708 (NC_000009.12:96778527::T 17504/120780) Row 332185709 (NC_000009.12:96778527::TT 6762/120800) Row 332185710 (NC_000009.12:96778527::TTT 208/120840)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 332185708 (NC_000009.12:96778527::T 17504/120780) Row 332185709 (NC_000009.12:96778527::TT 6762/120800) Row 332185710 (NC_000009.12:96778527::TTT 208/120840)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 332185708 (NC_000009.12:96778527::T 17504/120780) Row 332185709 (NC_000009.12:96778527::TT 6762/120800) Row 332185710 (NC_000009.12:96778527::TTT 208/120840)...	-	Apr 26, 2021 (155)
60	Korean Genome Project Submission ignored due to conflicting rows: Row 22747486 (NC_000009.12:96778527:TT: 160/1830) Row 22747487 (NC_000009.12:96778529::TT 317/1830) Row 22747488 (NC_000009.12:96778529::TTT 62/1830)...	-	Apr 26, 2020 (154)
61	Korean Genome Project Submission ignored due to conflicting rows: Row 22747486 (NC_000009.12:96778527:TT: 160/1830) Row 22747487 (NC_000009.12:96778529::TT 317/1830) Row 22747488 (NC_000009.12:96778529::TTT 62/1830)...	-	Apr 26, 2020 (154)
62	Korean Genome Project Submission ignored due to conflicting rows: Row 22747486 (NC_000009.12:96778527:TT: 160/1830) Row 22747487 (NC_000009.12:96778529::TT 317/1830) Row 22747488 (NC_000009.12:96778529::TTT 62/1830)...	-	Apr 26, 2020 (154)
63	Korean Genome Project Submission ignored due to conflicting rows: Row 22747486 (NC_000009.12:96778527:TT: 160/1830) Row 22747487 (NC_000009.12:96778529::TT 317/1830) Row 22747488 (NC_000009.12:96778529::TTT 62/1830)...	-	Apr 26, 2020 (154)
64	Korean Genome Project Submission ignored due to conflicting rows: Row 22747486 (NC_000009.12:96778527:TT: 160/1830) Row 22747487 (NC_000009.12:96778529::TT 317/1830) Row 22747488 (NC_000009.12:96778529::TTT 62/1830)...	-	Apr 26, 2020 (154)
65	8.3KJPN Submission ignored due to conflicting rows: Row 52410680 (NC_000009.11:99540809::TT 4312/16688) Row 52410681 (NC_000009.11:99540809:TT: 1201/16688) Row 52410682 (NC_000009.11:99540809::TTT 295/16688)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 52410680 (NC_000009.11:99540809::TT 4312/16688) Row 52410681 (NC_000009.11:99540809:TT: 1201/16688) Row 52410682 (NC_000009.11:99540809::TTT 295/16688)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 52410680 (NC_000009.11:99540809::TT 4312/16688) Row 52410681 (NC_000009.11:99540809:TT: 1201/16688) Row 52410682 (NC_000009.11:99540809::TTT 295/16688)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 52410680 (NC_000009.11:99540809::TT 4312/16688) Row 52410681 (NC_000009.11:99540809:TT: 1201/16688) Row 52410682 (NC_000009.11:99540809::TTT 295/16688)...	-	Apr 26, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 52410680 (NC_000009.11:99540809::TT 4312/16688) Row 52410681 (NC_000009.11:99540809:TT: 1201/16688) Row 52410682 (NC_000009.11:99540809::TTT 295/16688)...	-	Apr 26, 2021 (155)
70	14KJPN Submission ignored due to conflicting rows: Row 72558458 (NC_000009.12:96778527::TTT 424/27510) Row 72558459 (NC_000009.12:96778527::TT 6591/27510) Row 72558460 (NC_000009.12:96778527:TT: 2044/27510)...	-	Oct 13, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 72558458 (NC_000009.12:96778527::TTT 424/27510) Row 72558459 (NC_000009.12:96778527::TT 6591/27510) Row 72558460 (NC_000009.12:96778527:TT: 2044/27510)...	-	Oct 13, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 72558458 (NC_000009.12:96778527::TTT 424/27510) Row 72558459 (NC_000009.12:96778527::TT 6591/27510) Row 72558460 (NC_000009.12:96778527:TT: 2044/27510)...	-	Oct 13, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 72558458 (NC_000009.12:96778527::TTT 424/27510) Row 72558459 (NC_000009.12:96778527::TT 6591/27510) Row 72558460 (NC_000009.12:96778527:TT: 2044/27510)...	-	Oct 13, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 72558458 (NC_000009.12:96778527::TTT 424/27510) Row 72558459 (NC_000009.12:96778527::TT 6591/27510) Row 72558460 (NC_000009.12:96778527:TT: 2044/27510)...	-	Oct 13, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 72558458 (NC_000009.12:96778527::TTT 424/27510) Row 72558459 (NC_000009.12:96778527::TT 6591/27510) Row 72558460 (NC_000009.12:96778527:TT: 2044/27510)...	-	Oct 13, 2022 (156)
76	ALFA	NC_000009.12 - 96778528	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)
rs145389642	Sep 17, 2011 (135)
rs148582348	May 11, 2012 (137)
rs374047960	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4206168148	NC_000009.12:96778527:TTTTT:	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
2902472513	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4206168147	NC_000009.12:96778527:TTTT:	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
2902472513	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4206168146, ss5738721359	NC_000009.12:96778527:TTT:	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
2902472513	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss663945095, ss5194441374	NC_000009.11:99540809:TT:	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3966369485, ss4206168145, ss5281517463, ss5477450756, ss5738721356, ss5856854596	NC_000009.12:96778527:TT:	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
2902472513	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3005282254, ss3786472842, ss5194441377	NC_000009.11:99540809:T:	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4206168144, ss5477450754, ss5738721358	NC_000009.12:96778527:T:	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
2902472513	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3966369488	NC_000009.12:96778528:T:	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss295429999	NC_000009.10:98580631::T	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss295430000	NC_000009.10:98580647::T	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3831761542, ss5194441376	NC_000009.11:99540809::T	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4206168135, ss5281517464, ss5477450755, ss5738721357	NC_000009.12:96778527::T	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
2902472513	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3966369489	NC_000009.12:96778529::T	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss43434331	NT_008470.19:28705341::T	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss95521872	NT_008470.19:28705358::T	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5194441373	NC_000009.11:99540809::TT	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4206168136, ss5281517465, ss5477450752, ss5738721355	NC_000009.12:96778527::TT	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
2902472513	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3966369486	NC_000009.12:96778529::TT	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5194441375	NC_000009.11:99540809::TTT	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4206168137, ss5477450753, ss5738721354	NC_000009.12:96778527::TTT	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
2902472513	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3966369487	NC_000009.12:96778529::TTT	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4206168138	NC_000009.12:96778527::TTTT	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4206168139	NC_000009.12:96778527::TTTTT	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4206168140	NC_000009.12:96778527::TTTTTTT	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4206168141	NC_000009.12:96778527::TTTTTTTT	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4206168142	NC_000009.12:96778527::TTTTTTTTTT	NC_000009.12:96778527:TTTTTTTTTTTT… NC_000009.12:96778527:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs34111911

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

rs34111911