Name: rs34573245
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.

rs34573245

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:78623029-78623040 (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 / delTT / delT / dupT / du…
del(T)₄ / delTT / delT / dupT / dupTT / dupTTT
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.1782 (1539/8636, ALFA)
delT=0.3913 (1508/3854, ALSPAC)
delT=0.3943 (1462/3708, TWINSUK) (+ 3 more)
(T)₁₂=0.2186 (393/1798, 1000G)
(T)₁₂=0.50 (20/40, GENOME_DK)
delT=0.50 (20/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: None
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	8636	TTTTTTTTTTTT=0.8199	TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.1782, TTTTTTTTTTTTT=0.0012, TTTTTTTTTTTTTT=0.0007, TTTTTTTTTTTTTTT=0.0000	0.716012	0.071578	0.21241	32
European	Sub	7004	TTTTTTTTTTTT=0.7783	TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.2194, TTTTTTTTTTTTT=0.0014, TTTTTTTTTTTTTT=0.0009, TTTTTTTTTTTTTTT=0.0000	0.649842	0.088041	0.262116	32
African	Sub	906	TTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	34	TTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	872	TTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	52	TTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	36	TTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	16	TTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	74	TTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	344	TTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	56	TTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	200	TTTTTTTTTTTT=0.990	TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.010, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	0.99	0.01	0.0	32

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	8636	(T)₁₂=0.8199	del(T)₄=0.0000, delTT=0.0000, delT=0.1782, dupT=0.0012, dupTT=0.0007, dupTTT=0.0000
Allele Frequency Aggregator	European	Sub	7004	(T)₁₂=0.7783	del(T)₄=0.0000, delTT=0.0000, delT=0.2194, dupT=0.0014, dupTT=0.0009, dupTTT=0.0000
Allele Frequency Aggregator	African	Sub	906	(T)₁₂=1.000	del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	344	(T)₁₂=1.000	del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Other	Sub	200	(T)₁₂=0.990	del(T)₄=0.000, delTT=0.000, delT=0.010, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	74	(T)₁₂=1.00	del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	South Asian	Sub	56	(T)₁₂=1.00	del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Asian	Sub	52	(T)₁₂=1.00	del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(T)₁₂=0.6087	delT=0.3913
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	(T)₁₂=0.6057	delT=0.3943
1000Genomes	Global	Study-wide	1798	(T)₁₂=0.2186	delT=0.7814
1000Genomes	African	Sub	579	(T)₁₂=0.197	delT=0.803
1000Genomes	Europe	Sub	430	(T)₁₂=0.000	delT=1.000
1000Genomes	East Asian	Sub	338	(T)₁₂=0.787	delT=0.213
1000Genomes	South Asian	Sub	239	(T)₁₂=0.042	delT=0.958
1000Genomes	American	Sub	212	(T)₁₂=0.014	delT=0.986
The Danish reference pan genome	Danish	Study-wide	40	(T)₁₂=0.50	delT=0.50

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 15	NC_000015.10:g.78623037_78623040del
GRCh38.p14 chr 15	NC_000015.10:g.78623039_78623040del
GRCh38.p14 chr 15	NC_000015.10:g.78623040del
GRCh38.p14 chr 15	NC_000015.10:g.78623040dup
GRCh38.p14 chr 15	NC_000015.10:g.78623039_78623040dup
GRCh38.p14 chr 15	NC_000015.10:g.78623038_78623040dup
GRCh37.p13 chr 15	NC_000015.9:g.78915379_78915382del
GRCh37.p13 chr 15	NC_000015.9:g.78915381_78915382del
GRCh37.p13 chr 15	NC_000015.9:g.78915382del
GRCh37.p13 chr 15	NC_000015.9:g.78915382dup
GRCh37.p13 chr 15	NC_000015.9:g.78915381_78915382dup
GRCh37.p13 chr 15	NC_000015.9:g.78915380_78915382dup
CHRNA3 RefSeqGene	NG_016143.1:g.3264_3267del
CHRNA3 RefSeqGene	NG_016143.1:g.3266_3267del
CHRNA3 RefSeqGene	NG_016143.1:g.3267del
CHRNA3 RefSeqGene	NG_016143.1:g.3267dup
CHRNA3 RefSeqGene	NG_016143.1:g.3266_3267dup
CHRNA3 RefSeqGene	NG_016143.1:g.3265_3267dup

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)₁₂=	del(T)₄	delTT	delT	dupT	dupTT	dupTTT
GRCh38.p14 chr 15	NC_000015.10:g.78623029_78623040=	NC_000015.10:g.78623037_78623040del	NC_000015.10:g.78623039_78623040del	NC_000015.10:g.78623040del	NC_000015.10:g.78623040dup	NC_000015.10:g.78623039_78623040dup	NC_000015.10:g.78623038_78623040dup
GRCh37.p13 chr 15	NC_000015.9:g.78915371_78915382=	NC_000015.9:g.78915379_78915382del	NC_000015.9:g.78915381_78915382del	NC_000015.9:g.78915382del	NC_000015.9:g.78915382dup	NC_000015.9:g.78915381_78915382dup	NC_000015.9:g.78915380_78915382dup
CHRNA3 RefSeqGene	NG_016143.1:g.3256_3267=	NG_016143.1:g.3264_3267del	NG_016143.1:g.3266_3267del	NG_016143.1:g.3267del	NG_016143.1:g.3267dup	NG_016143.1:g.3266_3267dup	NG_016143.1:g.3265_3267dup

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#.

53 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40531816	Mar 14, 2006 (126)
2	HGSV	ss78010363	Sep 08, 2015 (146)
3	HGSV	ss83308499	Sep 08, 2015 (146)
4	HUMANGENOME_JCVI	ss95664507	Dec 05, 2013 (138)
5	BUSHMAN	ss193392705	Jul 04, 2010 (132)
6	GMI	ss289268329	May 04, 2012 (137)
7	PJP	ss294869260	May 09, 2011 (137)
8	SSMP	ss664288077	Apr 01, 2015 (144)
9	BILGI_BIOE	ss666655294	Apr 25, 2013 (138)
10	1000GENOMES	ss1375144695	Aug 21, 2014 (142)
11	1000GENOMES	ss1375144696	Aug 21, 2014 (142)
12	EVA_GENOME_DK	ss1574886217	Apr 01, 2015 (144)
13	EVA_UK10K_ALSPAC	ss1708368988	Apr 01, 2015 (144)
14	EVA_UK10K_TWINSUK	ss1708369248	Apr 01, 2015 (144)
15	HAMMER_LAB	ss1808288238	Sep 08, 2015 (146)
16	SWEGEN	ss3013594445	Nov 08, 2017 (151)
17	MCHAISSO	ss3065596910	Nov 08, 2017 (151)
18	BIOINF_KMB_FNS_UNIBA	ss3645393271	Oct 12, 2018 (152)
19	URBANLAB	ss3650397625	Oct 12, 2018 (152)
20	EVA_DECODE	ss3698270230	Jul 13, 2019 (153)
21	EVA_DECODE	ss3698270231	Jul 13, 2019 (153)
22	EVA_DECODE	ss3698270232	Jul 13, 2019 (153)
23	ACPOP	ss3741087769	Jul 13, 2019 (153)
24	ACPOP	ss3741087770	Jul 13, 2019 (153)
25	KHV_HUMAN_GENOMES	ss3818630180	Jul 13, 2019 (153)
26	KHV_HUMAN_GENOMES	ss3818630181	Jul 13, 2019 (153)
27	EVA	ss3834329421	Apr 27, 2020 (154)
28	EVA	ss3840764361	Apr 27, 2020 (154)
29	EVA	ss3846254352	Apr 27, 2020 (154)
30	KOGIC	ss3976541908	Apr 27, 2020 (154)
31	KOGIC	ss3976541909	Apr 27, 2020 (154)
32	KOGIC	ss3976541910	Apr 27, 2020 (154)
33	GNOMAD	ss4292149357	Apr 27, 2021 (155)
34	GNOMAD	ss4292149358	Apr 27, 2021 (155)
35	GNOMAD	ss4292149359	Apr 27, 2021 (155)
36	GNOMAD	ss4292149361	Apr 27, 2021 (155)
37	GNOMAD	ss4292149362	Apr 27, 2021 (155)
38	TOMMO_GENOMICS	ss5217095832	Apr 27, 2021 (155)
39	TOMMO_GENOMICS	ss5217095833	Apr 27, 2021 (155)
40	TOMMO_GENOMICS	ss5217095834	Apr 27, 2021 (155)
41	TOMMO_GENOMICS	ss5217095835	Apr 27, 2021 (155)
42	1000G_HIGH_COVERAGE	ss5299114507	Oct 16, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5299114508	Oct 16, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5299114509	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5492772099	Oct 16, 2022 (156)
46	HUGCELL_USP	ss5492772100	Oct 16, 2022 (156)
47	HUGCELL_USP	ss5492772101	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5771172402	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5771172403	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5771172404	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5771172405	Oct 16, 2022 (156)
52	EVA	ss5828461878	Oct 16, 2022 (156)
53	EVA	ss5949305959	Oct 16, 2022 (156)
54	1000Genomes	NC_000015.9 - 78915371	Oct 12, 2018 (152)
55	The Avon Longitudinal Study of Parents and Children	NC_000015.9 - 78915371	Oct 12, 2018 (152)
56	The Danish reference pan genome	NC_000015.9 - 78915371	Apr 27, 2020 (154)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474715873 (NC_000015.10:78623028::T 1164/135572) Row 474715874 (NC_000015.10:78623028::TT 5049/135562) Row 474715875 (NC_000015.10:78623028::TTT 17/135594)...	-	Apr 27, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474715873 (NC_000015.10:78623028::T 1164/135572) Row 474715874 (NC_000015.10:78623028::TT 5049/135562) Row 474715875 (NC_000015.10:78623028::TTT 17/135594)...	-	Apr 27, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474715873 (NC_000015.10:78623028::T 1164/135572) Row 474715874 (NC_000015.10:78623028::TT 5049/135562) Row 474715875 (NC_000015.10:78623028::TTT 17/135594)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474715873 (NC_000015.10:78623028::T 1164/135572) Row 474715874 (NC_000015.10:78623028::TT 5049/135562) Row 474715875 (NC_000015.10:78623028::TTT 17/135594)...	-	Apr 27, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 474715873 (NC_000015.10:78623028::T 1164/135572) Row 474715874 (NC_000015.10:78623028::TT 5049/135562) Row 474715875 (NC_000015.10:78623028::TTT 17/135594)...	-	Apr 27, 2021 (155)
62	Korean Genome Project Submission ignored due to conflicting rows: Row 32919909 (NC_000015.10:78623028:T: 163/1832) Row 32919910 (NC_000015.10:78623029::TT 471/1832) Row 32919911 (NC_000015.10:78623029::T 23/1832)	-	Apr 27, 2020 (154)
63	Korean Genome Project Submission ignored due to conflicting rows: Row 32919909 (NC_000015.10:78623028:T: 163/1832) Row 32919910 (NC_000015.10:78623029::TT 471/1832) Row 32919911 (NC_000015.10:78623029::T 23/1832)	-	Apr 27, 2020 (154)
64	Korean Genome Project Submission ignored due to conflicting rows: Row 32919909 (NC_000015.10:78623028:T: 163/1832) Row 32919910 (NC_000015.10:78623029::TT 471/1832) Row 32919911 (NC_000015.10:78623029::T 23/1832)	-	Apr 27, 2020 (154)
65	Northern Sweden Submission ignored due to conflicting rows: Row 14372634 (NC_000015.9:78915370:T: 213/598) Row 14372635 (NC_000015.9:78915370::T 2/598)	-	Jul 13, 2019 (153)
66	Northern Sweden Submission ignored due to conflicting rows: Row 14372634 (NC_000015.9:78915370:T: 213/598) Row 14372635 (NC_000015.9:78915370::T 2/598)	-	Jul 13, 2019 (153)
67	8.3KJPN Submission ignored due to conflicting rows: Row 75065139 (NC_000015.9:78915370::TT 4460/16756) Row 75065140 (NC_000015.9:78915370:T: 1188/16756) Row 75065141 (NC_000015.9:78915370::T 49/16756)...	-	Apr 27, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 75065139 (NC_000015.9:78915370::TT 4460/16756) Row 75065140 (NC_000015.9:78915370:T: 1188/16756) Row 75065141 (NC_000015.9:78915370::T 49/16756)...	-	Apr 27, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 75065139 (NC_000015.9:78915370::TT 4460/16756) Row 75065140 (NC_000015.9:78915370:T: 1188/16756) Row 75065141 (NC_000015.9:78915370::T 49/16756)...	-	Apr 27, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 75065139 (NC_000015.9:78915370::TT 4460/16756) Row 75065140 (NC_000015.9:78915370:T: 1188/16756) Row 75065141 (NC_000015.9:78915370::T 49/16756)...	-	Apr 27, 2021 (155)
71	14KJPN Submission ignored due to conflicting rows: Row 105009506 (NC_000015.10:78623028::TT 7673/28258) Row 105009507 (NC_000015.10:78623028:T: 1965/28258) Row 105009508 (NC_000015.10:78623028::T 78/28258)...	-	Oct 16, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 105009506 (NC_000015.10:78623028::TT 7673/28258) Row 105009507 (NC_000015.10:78623028:T: 1965/28258) Row 105009508 (NC_000015.10:78623028::T 78/28258)...	-	Oct 16, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 105009506 (NC_000015.10:78623028::TT 7673/28258) Row 105009507 (NC_000015.10:78623028:T: 1965/28258) Row 105009508 (NC_000015.10:78623028::T 78/28258)...	-	Oct 16, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 105009506 (NC_000015.10:78623028::TT 7673/28258) Row 105009507 (NC_000015.10:78623028:T: 1965/28258) Row 105009508 (NC_000015.10:78623028::T 78/28258)...	-	Oct 16, 2022 (156)
75	UK 10K study - Twins	NC_000015.9 - 78915371	Oct 12, 2018 (152)
76	ALFA	NC_000015.10 - 78623029	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)
rs55853939	May 11, 2012 (137)
rs61142951	May 26, 2008 (130)
rs375948194	May 13, 2013 (138)
rs374765100	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
5435467359	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTT	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTT	(self)
ss3698270230, ss4292149362	NC_000015.10:78623028:TT:	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTT	(self)
5435467359	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTT	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTT	(self)
ss78010363, ss83308499, ss294869260	NC_000015.8:76702436:T:	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
67331318, 37390264, 500768, 37390264, ss666655294, ss1375144695, ss1574886217, ss1708368988, ss1708369248, ss1808288238, ss3013594445, ss3741087769, ss3834329421, ss3840764361, ss5217095833, ss5828461878, ss5949305959	NC_000015.9:78915370:T:	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3065596910, ss3645393271, ss3650397625, ss3818630181, ss3846254352, ss3976541908, ss4292149361, ss5299114507, ss5492772099, ss5771172403	NC_000015.10:78623028:T:	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
5435467359	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTT	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3698270231	NC_000015.10:78623029:T:	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss40531816	NT_010194.17:49705927:T:	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss95664507	NT_010194.17:49705938:T:	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss193392705	NT_010194.18:55346154:T:	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3741087770, ss5217095834	NC_000015.9:78915370::T	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4292149357, ss5299114509, ss5492772100, ss5771172404	NC_000015.10:78623028::T	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
5435467359	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3976541910	NC_000015.10:78623029::T	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3698270232	NC_000015.10:78623030::T	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss289268329	NC_000015.8:76702437::TT	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss664288077, ss5217095832	NC_000015.9:78915370::TT	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss1375144696	NC_000015.9:78915371::TT	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4292149358, ss5299114508, ss5492772101, ss5771172402	NC_000015.10:78623028::TT	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
5435467359	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3818630180, ss3976541909	NC_000015.10:78623029::TT	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss5217095835	NC_000015.9:78915370::TTT	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4292149359, ss5771172405	NC_000015.10:78623028::TTT	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
5435467359	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000015.10:78623028:TTTTTTTTTTTT… NC_000015.10:78623028:TTTTTTTTTTTT:TTTTTTTTTTTTTTT	(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 rs34573245

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

rs34573245