Name: rs34097461
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.

rs34097461

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:177410301-177410317 (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)₉
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.2584 (1630/6308, ALFA)
(T)₁₇=0.4958 (2483/5008, 1000G)
(T)₁₇=0.1497 (577/3854, ALSPAC) (+ 1 more)
(T)₁₇=0.1729 (641/3708, TWINSUK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SLC34A1 : Intron Variant
F12 : 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	6308	TTTTTTTTTTTTTTTTT=0.7400	TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0002, TTTTTTTTTTTTTTTT=0.2584, TTTTTTTTTTTTTTTTTT=0.0014, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000	0.626391	0.142766	0.230843	32
European	Sub	5242	TTTTTTTTTTTTTTTTT=0.6873	TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0002, TTTTTTTTTTTTTTTT=0.3108, TTTTTTTTTTTTTTTTTT=0.0017, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000	0.550536	0.171899	0.277565	32
African	Sub	718	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	22	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	696	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	76	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	56	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	20	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	14	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	124	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	26	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	108	TTTTTTTTTTTTTTTTT=0.991	TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.009, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	0.981481	0.0	0.018519	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	6308	(T)₁₇=0.7400	delTTT=0.0000, delTT=0.0002, delT=0.2584, dupT=0.0014, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	European	Sub	5242	(T)₁₇=0.6873	delTTT=0.0000, delTT=0.0002, delT=0.3108, dupT=0.0017, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	African	Sub	718	(T)₁₇=1.000	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	Latin American 2	Sub	124	(T)₁₇=1.000	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	108	(T)₁₇=0.991	delTTT=0.000, delTT=0.000, delT=0.009, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Asian	Sub	76	(T)₁₇=1.00	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	26	(T)₁₇=1.00	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	14	(T)₁₇=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
1000Genomes	Global	Study-wide	5008	(T)₁₇=0.4958	delT=0.5042
1000Genomes	African	Sub	1322	(T)₁₇=0.4728	delT=0.5272
1000Genomes	East Asian	Sub	1008	(T)₁₇=0.7014	delT=0.2986
1000Genomes	Europe	Sub	1006	(T)₁₇=0.3360	delT=0.6640
1000Genomes	South Asian	Sub	978	(T)₁₇=0.534	delT=0.466
1000Genomes	American	Sub	694	(T)₁₇=0.419	delT=0.581
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(T)₁₇=0.1497	delT=0.8503
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	(T)₁₇=0.1729	delT=0.8271

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 5	NC_000005.10:g.177410313_177410317del
GRCh38.p14 chr 5	NC_000005.10:g.177410314_177410317del
GRCh38.p14 chr 5	NC_000005.10:g.177410315_177410317del
GRCh38.p14 chr 5	NC_000005.10:g.177410316_177410317del
GRCh38.p14 chr 5	NC_000005.10:g.177410317del
GRCh38.p14 chr 5	NC_000005.10:g.177410317dup
GRCh38.p14 chr 5	NC_000005.10:g.177410316_177410317dup
GRCh38.p14 chr 5	NC_000005.10:g.177410315_177410317dup
GRCh38.p14 chr 5	NC_000005.10:g.177410314_177410317dup
GRCh38.p14 chr 5	NC_000005.10:g.177410309_177410317dup
GRCh37.p13 chr 5	NC_000005.9:g.176837314_176837318del
GRCh37.p13 chr 5	NC_000005.9:g.176837315_176837318del
GRCh37.p13 chr 5	NC_000005.9:g.176837316_176837318del
GRCh37.p13 chr 5	NC_000005.9:g.176837317_176837318del
GRCh37.p13 chr 5	NC_000005.9:g.176837318del
GRCh37.p13 chr 5	NC_000005.9:g.176837318dup
GRCh37.p13 chr 5	NC_000005.9:g.176837317_176837318dup
GRCh37.p13 chr 5	NC_000005.9:g.176837316_176837318dup
GRCh37.p13 chr 5	NC_000005.9:g.176837315_176837318dup
GRCh37.p13 chr 5	NC_000005.9:g.176837310_176837318dup
F12 RefSeqGene (LRG_145)	NG_007568.1:g.4272_4276del
F12 RefSeqGene (LRG_145)	NG_007568.1:g.4273_4276del
F12 RefSeqGene (LRG_145)	NG_007568.1:g.4274_4276del
F12 RefSeqGene (LRG_145)	NG_007568.1:g.4275_4276del
F12 RefSeqGene (LRG_145)	NG_007568.1:g.4276del
F12 RefSeqGene (LRG_145)	NG_007568.1:g.4276dup
F12 RefSeqGene (LRG_145)	NG_007568.1:g.4275_4276dup
F12 RefSeqGene (LRG_145)	NG_007568.1:g.4274_4276dup
F12 RefSeqGene (LRG_145)	NG_007568.1:g.4273_4276dup
F12 RefSeqGene (LRG_145)	NG_007568.1:g.4268_4276dup

Gene: SLC34A1, solute carrier family 34 member 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SLC34A1 transcript variant 2	NM_001167579.2:c.	N/A	Genic Downstream Transcript Variant
SLC34A1 transcript variant 1	NM_003052.5:c.	N/A	Genic Downstream Transcript Variant
SLC34A1 transcript variant X2	XM_017009773.2:c.1417-145… XM_017009773.2:c.1417-1451_1417-1447del	N/A	Intron Variant
SLC34A1 transcript variant X4	XM_017009774.2:c.	N/A	Genic Downstream Transcript Variant
SLC34A1 transcript variant X5	XM_017009775.2:c.	N/A	Genic Downstream Transcript Variant
SLC34A1 transcript variant X1	XM_024446191.1:c.	N/A	Genic Downstream Transcript Variant
SLC34A1 transcript variant X3	XR_941113.3:n.	N/A	Genic Downstream Transcript Variant

Gene: F12, coagulation factor XII (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
F12 transcript	NM_000505.4:c.	N/A	Upstream Transcript Variant
F12 transcript variant X1	XM_011534462.3: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)₉
GRCh38.p14 chr 5	NC_000005.10:g.177410301_177410317=	NC_000005.10:g.177410313_177410317del	NC_000005.10:g.177410314_177410317del	NC_000005.10:g.177410315_177410317del	NC_000005.10:g.177410316_177410317del	NC_000005.10:g.177410317del	NC_000005.10:g.177410317dup	NC_000005.10:g.177410316_177410317dup	NC_000005.10:g.177410315_177410317dup	NC_000005.10:g.177410314_177410317dup	NC_000005.10:g.177410309_177410317dup
GRCh37.p13 chr 5	NC_000005.9:g.176837302_176837318=	NC_000005.9:g.176837314_176837318del	NC_000005.9:g.176837315_176837318del	NC_000005.9:g.176837316_176837318del	NC_000005.9:g.176837317_176837318del	NC_000005.9:g.176837318del	NC_000005.9:g.176837318dup	NC_000005.9:g.176837317_176837318dup	NC_000005.9:g.176837316_176837318dup	NC_000005.9:g.176837315_176837318dup	NC_000005.9:g.176837310_176837318dup
F12 RefSeqGene (LRG_145)	NG_007568.1:g.4260_4276=	NG_007568.1:g.4272_4276del	NG_007568.1:g.4273_4276del	NG_007568.1:g.4274_4276del	NG_007568.1:g.4275_4276del	NG_007568.1:g.4276del	NG_007568.1:g.4276dup	NG_007568.1:g.4275_4276dup	NG_007568.1:g.4274_4276dup	NG_007568.1:g.4273_4276dup	NG_007568.1:g.4268_4276dup
SLC34A1 transcript variant X2	XM_017009773.2:c.1417-1463=	XM_017009773.2:c.1417-1451_1417-1447del	XM_017009773.2:c.1417-1450_1417-1447del	XM_017009773.2:c.1417-1449_1417-1447del	XM_017009773.2:c.1417-1448_1417-1447del	XM_017009773.2:c.1417-1447del	XM_017009773.2:c.1417-1447dup	XM_017009773.2:c.1417-1448_1417-1447dup	XM_017009773.2:c.1417-1449_1417-1447dup	XM_017009773.2:c.1417-1450_1417-1447dup	XM_017009773.2:c.1417-1455_1417-1447dup

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#.

42 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42529668	Mar 13, 2006 (126)
2	HUMANGENOME_JCVI	ss95415499	Feb 05, 2009 (130)
3	1000GENOMES	ss1374909292	Aug 21, 2014 (142)
4	EVA_UK10K_ALSPAC	ss1704991253	Apr 01, 2015 (144)
5	EVA_UK10K_TWINSUK	ss1704991254	Apr 01, 2015 (144)
6	SWEGEN	ss2998316746	Nov 08, 2017 (151)
7	MCHAISSO	ss3064186926	Nov 08, 2017 (151)
8	MCHAISSO	ss3065063085	Nov 08, 2017 (151)
9	EVA_DECODE	ss3716343725	Jul 13, 2019 (153)
10	EVA_DECODE	ss3716343726	Jul 13, 2019 (153)
11	EVA_DECODE	ss3716343727	Jul 13, 2019 (153)
12	EVA_DECODE	ss3716343728	Jul 13, 2019 (153)
13	EVA_DECODE	ss3716343729	Jul 13, 2019 (153)
14	PACBIO	ss3785337128	Jul 13, 2019 (153)
15	PACBIO	ss3790706655	Jul 13, 2019 (153)
16	PACBIO	ss3795583851	Jul 13, 2019 (153)
17	KHV_HUMAN_GENOMES	ss3807625732	Jul 13, 2019 (153)
18	EVA	ss3829666827	Apr 26, 2020 (154)
19	GNOMAD	ss4135003391	Apr 26, 2021 (155)
20	GNOMAD	ss4135003392	Apr 26, 2021 (155)
21	GNOMAD	ss4135003393	Apr 26, 2021 (155)
22	GNOMAD	ss4135003394	Apr 26, 2021 (155)
23	GNOMAD	ss4135003396	Apr 26, 2021 (155)
24	GNOMAD	ss4135003397	Apr 26, 2021 (155)
25	GNOMAD	ss4135003398	Apr 26, 2021 (155)
26	GNOMAD	ss4135003399	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5175618373	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5175618374	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5175618375	Apr 26, 2021 (155)
30	1000G_HIGH_COVERAGE	ss5266983813	Oct 13, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5266983814	Oct 13, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5266983815	Oct 13, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5266983816	Oct 13, 2022 (156)
34	HUGCELL_USP	ss5464829092	Oct 13, 2022 (156)
35	HUGCELL_USP	ss5464829093	Oct 13, 2022 (156)
36	HUGCELL_USP	ss5464829094	Oct 13, 2022 (156)
37	TOMMO_GENOMICS	ss5713122831	Oct 13, 2022 (156)
38	TOMMO_GENOMICS	ss5713122832	Oct 13, 2022 (156)
39	TOMMO_GENOMICS	ss5713122833	Oct 13, 2022 (156)
40	EVA	ss5855150137	Oct 13, 2022 (156)
41	EVA	ss5968024990	Oct 13, 2022 (156)
42	EVA	ss5980333557	Oct 13, 2022 (156)
43	1000Genomes	NC_000005.9 - 176837302	Oct 12, 2018 (152)
44	The Avon Longitudinal Study of Parents and Children	NC_000005.9 - 176837302	Oct 12, 2018 (152)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 213833692 (NC_000005.10:177410300::T 551/102490) Row 213833693 (NC_000005.10:177410300::TT 1/102498) Row 213833694 (NC_000005.10:177410300::TTT 41/102498)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 213833692 (NC_000005.10:177410300::T 551/102490) Row 213833693 (NC_000005.10:177410300::TT 1/102498) Row 213833694 (NC_000005.10:177410300::TTT 41/102498)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 213833692 (NC_000005.10:177410300::T 551/102490) Row 213833693 (NC_000005.10:177410300::TT 1/102498) Row 213833694 (NC_000005.10:177410300::TTT 41/102498)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 213833692 (NC_000005.10:177410300::T 551/102490) Row 213833693 (NC_000005.10:177410300::TT 1/102498) Row 213833694 (NC_000005.10:177410300::TTT 41/102498)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 213833692 (NC_000005.10:177410300::T 551/102490) Row 213833693 (NC_000005.10:177410300::TT 1/102498) Row 213833694 (NC_000005.10:177410300::TTT 41/102498)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 213833692 (NC_000005.10:177410300::T 551/102490) Row 213833693 (NC_000005.10:177410300::TT 1/102498) Row 213833694 (NC_000005.10:177410300::TTT 41/102498)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 213833692 (NC_000005.10:177410300::T 551/102490) Row 213833693 (NC_000005.10:177410300::TT 1/102498) Row 213833694 (NC_000005.10:177410300::TTT 41/102498)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 213833692 (NC_000005.10:177410300::T 551/102490) Row 213833693 (NC_000005.10:177410300::TT 1/102498) Row 213833694 (NC_000005.10:177410300::TTT 41/102498)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 213833692 (NC_000005.10:177410300::T 551/102490) Row 213833693 (NC_000005.10:177410300::TT 1/102498) Row 213833694 (NC_000005.10:177410300::TTT 41/102498)...	-	Apr 26, 2021 (155)
54	8.3KJPN Submission ignored due to conflicting rows: Row 33587680 (NC_000005.9:176837301:T: 4103/16242) Row 33587681 (NC_000005.9:176837301::T 96/16242) Row 33587682 (NC_000005.9:176837301:TT: 5/16242)	-	Apr 26, 2021 (155)
55	8.3KJPN Submission ignored due to conflicting rows: Row 33587680 (NC_000005.9:176837301:T: 4103/16242) Row 33587681 (NC_000005.9:176837301::T 96/16242) Row 33587682 (NC_000005.9:176837301:TT: 5/16242)	-	Apr 26, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 33587680 (NC_000005.9:176837301:T: 4103/16242) Row 33587681 (NC_000005.9:176837301::T 96/16242) Row 33587682 (NC_000005.9:176837301:TT: 5/16242)	-	Apr 26, 2021 (155)
57	14KJPN Submission ignored due to conflicting rows: Row 46959935 (NC_000005.10:177410300:T: 8017/28166) Row 46959936 (NC_000005.10:177410300::T 178/28166) Row 46959937 (NC_000005.10:177410300:TT: 4/28166)	-	Oct 13, 2022 (156)
58	14KJPN Submission ignored due to conflicting rows: Row 46959935 (NC_000005.10:177410300:T: 8017/28166) Row 46959936 (NC_000005.10:177410300::T 178/28166) Row 46959937 (NC_000005.10:177410300:TT: 4/28166)	-	Oct 13, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 46959935 (NC_000005.10:177410300:T: 8017/28166) Row 46959936 (NC_000005.10:177410300::T 178/28166) Row 46959937 (NC_000005.10:177410300:TT: 4/28166)	-	Oct 13, 2022 (156)
60	UK 10K study - Twins	NC_000005.9 - 176837302	Oct 12, 2018 (152)
61	ALFA	NC_000005.10 - 177410301	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
ss5980333557	NC_000005.9:176837301:TTTTT:	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT
ss4135003399	NC_000005.10:177410300:TTTTT:	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4135003398	NC_000005.10:177410300:TTTT:	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3716343725, ss4135003397	NC_000005.10:177410300:TTT:	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
6637311919	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss5175618375	NC_000005.9:176837301:TT:	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4135003396, ss5266983814, ss5464829093, ss5713122833	NC_000005.10:177410300:TT:	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
6637311919	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3716343726	NC_000005.10:177410301:TT:	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
30235216, 16835010, 16835010, ss1374909292, ss1704991253, ss1704991254, ss2998316746, ss3785337128, ss3790706655, ss3795583851, ss3829666827, ss5175618373, ss5968024990	NC_000005.9:176837301:T:	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3064186926, ss3065063085, ss3807625732, ss5266983813, ss5464829092, ss5713122831, ss5855150137	NC_000005.10:177410300:T:	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
6637311919	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3716343727	NC_000005.10:177410302:T:	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss42529668, ss95415499	NT_023133.13:21648590:T:	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss5175618374	NC_000005.9:176837301::T	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4135003391, ss5266983815, ss5464829094, ss5713122832	NC_000005.10:177410300::T	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
6637311919	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3716343728	NC_000005.10:177410303::T	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4135003392	NC_000005.10:177410300::TT	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
6637311919	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4135003393, ss5266983816	NC_000005.10:177410300::TTT	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
6637311919	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4135003394	NC_000005.10:177410300::TTTT	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
6637311919	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3716343729	NC_000005.10:177410303::TTTTTTTTT	NC_000005.10:177410300:TTTTTTTTTTT… NC_000005.10:177410300:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs34097461

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

rs34097461