Name: rs71098673
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.

rs71098673

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:108322750-108322764 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₄ / delTTT / delTT / delT / …
del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₉
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.05006 (542/10828, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LOC124905416 : Intron 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	10828	TTTTTTTTTTTTTTT=0.93942	TTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.01053, TTTTTTTTTTTTTTTT=0.05006, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000	0.913806	0.013768	0.072425	32
European	Sub	8656	TTTTTTTTTTTTTTT=0.9246	TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0131, TTTTTTTTTTTTTTTT=0.0624, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000	0.892103	0.017311	0.090586	32
African	Sub	1338	TTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	36	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1302	TTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	60	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	40	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	20	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	68	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	364	TTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	64	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	278	TTTTTTTTTTTTTTT=0.989	TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.004, TTTTTTTTTTTTTTTT=0.007, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	0.985507	0.0	0.014493	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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	10828	(T)₁₅=0.93942	del(T)₄=0.00000, delTT=0.00000, delT=0.01053, dupT=0.05006, dupTT=0.00000, dupTTT=0.00000, dup(T)₄=0.00000
Allele Frequency Aggregator	European	Sub	8656	(T)₁₅=0.9246	del(T)₄=0.0000, delTT=0.0000, delT=0.0131, dupT=0.0624, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	African	Sub	1338	(T)₁₅=1.0000	del(T)₄=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	364	(T)₁₅=1.000	del(T)₄=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	278	(T)₁₅=0.989	del(T)₄=0.000, delTT=0.000, delT=0.004, dupT=0.007, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	68	(T)₁₅=1.00	del(T)₄=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	64	(T)₁₅=1.00	del(T)₄=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	Asian	Sub	60	(T)₁₅=1.00	del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 1	NC_000001.11:g.108322761_108322764del
GRCh38.p14 chr 1	NC_000001.11:g.108322762_108322764del
GRCh38.p14 chr 1	NC_000001.11:g.108322763_108322764del
GRCh38.p14 chr 1	NC_000001.11:g.108322764del
GRCh38.p14 chr 1	NC_000001.11:g.108322764dup
GRCh38.p14 chr 1	NC_000001.11:g.108322763_108322764dup
GRCh38.p14 chr 1	NC_000001.11:g.108322762_108322764dup
GRCh38.p14 chr 1	NC_000001.11:g.108322761_108322764dup
GRCh38.p14 chr 1	NC_000001.11:g.108322756_108322764dup
GRCh37.p13 chr 1	NC_000001.10:g.108865383_108865386del
GRCh37.p13 chr 1	NC_000001.10:g.108865384_108865386del
GRCh37.p13 chr 1	NC_000001.10:g.108865385_108865386del
GRCh37.p13 chr 1	NC_000001.10:g.108865386del
GRCh37.p13 chr 1	NC_000001.10:g.108865386dup
GRCh37.p13 chr 1	NC_000001.10:g.108865385_108865386dup
GRCh37.p13 chr 1	NC_000001.10:g.108865384_108865386dup
GRCh37.p13 chr 1	NC_000001.10:g.108865383_108865386dup
GRCh37.p13 chr 1	NC_000001.10:g.108865378_108865386dup
SLC25A24P1 pseudogene	NG_027806.2:g.49723_49726del
SLC25A24P1 pseudogene	NG_027806.2:g.49724_49726del
SLC25A24P1 pseudogene	NG_027806.2:g.49725_49726del
SLC25A24P1 pseudogene	NG_027806.2:g.49726del
SLC25A24P1 pseudogene	NG_027806.2:g.49726dup
SLC25A24P1 pseudogene	NG_027806.2:g.49725_49726dup
SLC25A24P1 pseudogene	NG_027806.2:g.49724_49726dup
SLC25A24P1 pseudogene	NG_027806.2:g.49723_49726dup
SLC25A24P1 pseudogene	NG_027806.2:g.49718_49726dup
GRCh38.p14 chr 1 novel patch HSCHR1_6_CTG3	NW_017852928.1:g.383462_383465del
GRCh38.p14 chr 1 novel patch HSCHR1_6_CTG3	NW_017852928.1:g.383463_383465del
GRCh38.p14 chr 1 novel patch HSCHR1_6_CTG3	NW_017852928.1:g.383464_383465del
GRCh38.p14 chr 1 novel patch HSCHR1_6_CTG3	NW_017852928.1:g.383465del
GRCh38.p14 chr 1 novel patch HSCHR1_6_CTG3	NW_017852928.1:g.383465dup
GRCh38.p14 chr 1 novel patch HSCHR1_6_CTG3	NW_017852928.1:g.383464_383465dup
GRCh38.p14 chr 1 novel patch HSCHR1_6_CTG3	NW_017852928.1:g.383463_383465dup
GRCh38.p14 chr 1 novel patch HSCHR1_6_CTG3	NW_017852928.1:g.383462_383465dup
GRCh38.p14 chr 1 novel patch HSCHR1_6_CTG3	NW_017852928.1:g.383457_383465dup

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

Not Reported in ClinVar

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

Placement	(T)₁₅=	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₉
GRCh38.p14 chr 1	NC_000001.11:g.108322750_108322764=	NC_000001.11:g.108322761_108322764del	NC_000001.11:g.108322762_108322764del	NC_000001.11:g.108322763_108322764del	NC_000001.11:g.108322764del	NC_000001.11:g.108322764dup	NC_000001.11:g.108322763_108322764dup	NC_000001.11:g.108322762_108322764dup	NC_000001.11:g.108322761_108322764dup	NC_000001.11:g.108322756_108322764dup
GRCh37.p13 chr 1	NC_000001.10:g.108865372_108865386=	NC_000001.10:g.108865383_108865386del	NC_000001.10:g.108865384_108865386del	NC_000001.10:g.108865385_108865386del	NC_000001.10:g.108865386del	NC_000001.10:g.108865386dup	NC_000001.10:g.108865385_108865386dup	NC_000001.10:g.108865384_108865386dup	NC_000001.10:g.108865383_108865386dup	NC_000001.10:g.108865378_108865386dup
SLC25A24P1 pseudogene	NG_027806.2:g.49712_49726=	NG_027806.2:g.49723_49726del	NG_027806.2:g.49724_49726del	NG_027806.2:g.49725_49726del	NG_027806.2:g.49726del	NG_027806.2:g.49726dup	NG_027806.2:g.49725_49726dup	NG_027806.2:g.49724_49726dup	NG_027806.2:g.49723_49726dup	NG_027806.2:g.49718_49726dup
GRCh38.p14 chr 1 novel patch HSCHR1_6_CTG3	NW_017852928.1:g.383451_383465=	NW_017852928.1:g.383462_383465del	NW_017852928.1:g.383463_383465del	NW_017852928.1:g.383464_383465del	NW_017852928.1:g.383465del	NW_017852928.1:g.383465dup	NW_017852928.1:g.383464_383465dup	NW_017852928.1:g.383463_383465dup	NW_017852928.1:g.383462_383465dup	NW_017852928.1:g.383457_383465dup

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#.

33 SubSNP, 14 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95239820	Dec 05, 2013 (138)
2	PJP	ss294597532	May 09, 2011 (137)
3	SWEGEN	ss2987406343	Nov 08, 2017 (151)
4	MCHAISSO	ss3065320658	Nov 08, 2017 (151)
5	URBANLAB	ss3646747815	Oct 11, 2018 (152)
6	EVA_DECODE	ss3687491564	Jul 12, 2019 (153)
7	EVA_DECODE	ss3687491565	Jul 12, 2019 (153)
8	EVA_DECODE	ss3687491566	Jul 12, 2019 (153)
9	EVA_DECODE	ss3687491567	Jul 12, 2019 (153)
10	EVA_DECODE	ss3687491568	Jul 12, 2019 (153)
11	PACBIO	ss3783514129	Jul 12, 2019 (153)
12	EVA	ss3826359317	Apr 25, 2020 (154)
13	GNOMAD	ss4000100577	Apr 25, 2021 (155)
14	GNOMAD	ss4000100578	Apr 25, 2021 (155)
15	GNOMAD	ss4000100579	Apr 25, 2021 (155)
16	GNOMAD	ss4000100580	Apr 25, 2021 (155)
17	GNOMAD	ss4000100581	Apr 25, 2021 (155)
18	GNOMAD	ss4000100582	Apr 25, 2021 (155)
19	GNOMAD	ss4000100583	Apr 25, 2021 (155)
20	TOMMO_GENOMICS	ss5145591582	Apr 25, 2021 (155)
21	TOMMO_GENOMICS	ss5145591583	Apr 25, 2021 (155)
22	TOMMO_GENOMICS	ss5145591584	Apr 25, 2021 (155)
23	1000G_HIGH_COVERAGE	ss5243542691	Oct 12, 2022 (156)
24	1000G_HIGH_COVERAGE	ss5243542692	Oct 12, 2022 (156)
25	1000G_HIGH_COVERAGE	ss5243542693	Oct 12, 2022 (156)
26	1000G_HIGH_COVERAGE	ss5243542694	Oct 12, 2022 (156)
27	HUGCELL_USP	ss5444473919	Oct 12, 2022 (156)
28	HUGCELL_USP	ss5444473920	Oct 12, 2022 (156)
29	HUGCELL_USP	ss5444473921	Oct 12, 2022 (156)
30	TOMMO_GENOMICS	ss5670832633	Oct 12, 2022 (156)
31	TOMMO_GENOMICS	ss5670832634	Oct 12, 2022 (156)
32	TOMMO_GENOMICS	ss5670832635	Oct 12, 2022 (156)
33	EVA	ss5849060370	Oct 12, 2022 (156)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22126615 (NC_000001.11:108322749::T 24032/91724) Row 22126616 (NC_000001.11:108322749::TT 206/91836) Row 22126617 (NC_000001.11:108322749::TTT 1/91840)...	-	Apr 25, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22126615 (NC_000001.11:108322749::T 24032/91724) Row 22126616 (NC_000001.11:108322749::TT 206/91836) Row 22126617 (NC_000001.11:108322749::TTT 1/91840)...	-	Apr 25, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22126615 (NC_000001.11:108322749::T 24032/91724) Row 22126616 (NC_000001.11:108322749::TT 206/91836) Row 22126617 (NC_000001.11:108322749::TTT 1/91840)...	-	Apr 25, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22126615 (NC_000001.11:108322749::T 24032/91724) Row 22126616 (NC_000001.11:108322749::TT 206/91836) Row 22126617 (NC_000001.11:108322749::TTT 1/91840)...	-	Apr 25, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22126615 (NC_000001.11:108322749::T 24032/91724) Row 22126616 (NC_000001.11:108322749::TT 206/91836) Row 22126617 (NC_000001.11:108322749::TTT 1/91840)...	-	Apr 25, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22126615 (NC_000001.11:108322749::T 24032/91724) Row 22126616 (NC_000001.11:108322749::TT 206/91836) Row 22126617 (NC_000001.11:108322749::TTT 1/91840)...	-	Apr 25, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22126615 (NC_000001.11:108322749::T 24032/91724) Row 22126616 (NC_000001.11:108322749::TT 206/91836) Row 22126617 (NC_000001.11:108322749::TTT 1/91840)...	-	Apr 25, 2021 (155)
41	8.3KJPN Submission ignored due to conflicting rows: Row 3560889 (NC_000001.10:108865371::T 4720/16606) Row 3560890 (NC_000001.10:108865371:T: 7/16606) Row 3560891 (NC_000001.10:108865371::TT 10/16606)	-	Apr 25, 2021 (155)
42	8.3KJPN Submission ignored due to conflicting rows: Row 3560889 (NC_000001.10:108865371::T 4720/16606) Row 3560890 (NC_000001.10:108865371:T: 7/16606) Row 3560891 (NC_000001.10:108865371::TT 10/16606)	-	Apr 25, 2021 (155)
43	8.3KJPN Submission ignored due to conflicting rows: Row 3560889 (NC_000001.10:108865371::T 4720/16606) Row 3560890 (NC_000001.10:108865371:T: 7/16606) Row 3560891 (NC_000001.10:108865371::TT 10/16606)	-	Apr 25, 2021 (155)
44	14KJPN Submission ignored due to conflicting rows: Row 4669737 (NC_000001.11:108322749::T 8130/28248) Row 4669738 (NC_000001.11:108322749:T: 10/28248) Row 4669739 (NC_000001.11:108322749::TT 14/28248)	-	Oct 12, 2022 (156)
45	14KJPN Submission ignored due to conflicting rows: Row 4669737 (NC_000001.11:108322749::T 8130/28248) Row 4669738 (NC_000001.11:108322749:T: 10/28248) Row 4669739 (NC_000001.11:108322749::TT 14/28248)	-	Oct 12, 2022 (156)
46	14KJPN Submission ignored due to conflicting rows: Row 4669737 (NC_000001.11:108322749::T 8130/28248) Row 4669738 (NC_000001.11:108322749:T: 10/28248) Row 4669739 (NC_000001.11:108322749::TT 14/28248)	-	Oct 12, 2022 (156)
47	ALFA	NC_000001.11 - 108322750	Apr 25, 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)
rs139237386	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4000100583	NC_000001.11:108322749:TTTT:	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
15165518129	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4000100582	NC_000001.11:108322749:TTT:	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3687491564, ss4000100581, ss5243542694	NC_000001.11:108322749:TT:	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
15165518129	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss2987406343, ss3783514129, ss5145591583	NC_000001.10:108865371:T:	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3065320658, ss4000100580, ss5243542691, ss5444473919, ss5670832634	NC_000001.11:108322749:T:	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
15165518129	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3687491565	NC_000001.11:108322750:T:	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss294597532	NC_000001.9:108666895::T	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3826359317, ss5145591582	NC_000001.10:108865371::T	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3646747815, ss4000100577, ss5243542692, ss5444473920, ss5670832633, ss5849060370	NC_000001.11:108322749::T	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
15165518129	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3687491566	NC_000001.11:108322751::T	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss95239820	NT_032977.9:78837304::T	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss5145591584	NC_000001.10:108865371::TT	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4000100578, ss5243542693, ss5444473921, ss5670832635	NC_000001.11:108322749::TT	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
15165518129	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3687491567	NC_000001.11:108322751::TT	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4000100579	NC_000001.11:108322749::TTT	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
15165518129	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
15165518129	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3687491568	NC_000001.11:108322751::TTTTTTTTT	NC_000001.11:108322749:TTTTTTTTTTT… NC_000001.11:108322749:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(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 rs71098673

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

rs71098673