Name: rs34469545
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.

rs34469545

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:131211603-131211615 (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: delTTT / delTT / delT / dupT / dup…
delTTT / delTT / delT / dupT / dupTT
Variation Type: Indel Insertion and Deletion
Frequency: delTT=0.1158 (1091/9422, ALFA)
delTT=0.1112 (468/4210, 1000G)
delTT=0.2206 (850/3854, ALSPAC)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MKLN1 : 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	9422	TTTTTTTTTTTTT=0.8194	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.1158, TTTTTTTTTTTT=0.0604, TTTTTTTTTTTTTT=0.0045, TTTTTTTTTTTTTTT=0.0000	0.805042	0.035774	0.159184	32
European	Sub	7218	TTTTTTTTTTTTT=0.7642	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.1511, TTTTTTTTTTTT=0.0788, TTTTTTTTTTTTTT=0.0058, TTTTTTTTTTTTTTT=0.0000	0.7349	0.048645	0.216454	32
African	Sub	1506	TTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	48	TTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1458	TTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	74	TTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	52	TTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	22	TTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	72	TTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	262	TTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	60	TTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	230	TTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=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	9422	(T)₁₃=0.8194	delTTT=0.0000, delTT=0.1158, delT=0.0604, dupT=0.0045, dupTT=0.0000
Allele Frequency Aggregator	European	Sub	7218	(T)₁₃=0.7642	delTTT=0.0000, delTT=0.1511, delT=0.0788, dupT=0.0058, dupTT=0.0000
Allele Frequency Aggregator	African	Sub	1506	(T)₁₃=1.0000	delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	262	(T)₁₃=1.000	delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Other	Sub	230	(T)₁₃=1.000	delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Asian	Sub	74	(T)₁₃=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Latin American 1	Sub	72	(T)₁₃=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	South Asian	Sub	60	(T)₁₃=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
1000Genomes	Global	Study-wide	4210	(T)₁₃=0.8888	delTT=0.1112
1000Genomes	African	Sub	1046	(T)₁₃=0.8967	delTT=0.1033
1000Genomes	East Asian	Sub	939	(T)₁₃=0.978	delTT=0.022
1000Genomes	Europe	Sub	860	(T)₁₃=0.781	delTT=0.219
1000Genomes	South Asian	Sub	836	(T)₁₃=0.925	delTT=0.075
1000Genomes	American	Sub	529	(T)₁₃=0.834	delTT=0.166
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(T)₁₃=0.7794	delTT=0.2206

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 7	NC_000007.14:g.131211613_131211615del
GRCh38.p14 chr 7	NC_000007.14:g.131211614_131211615del
GRCh38.p14 chr 7	NC_000007.14:g.131211615del
GRCh38.p14 chr 7	NC_000007.14:g.131211615dup
GRCh38.p14 chr 7	NC_000007.14:g.131211614_131211615dup
GRCh37.p13 chr 7	NC_000007.13:g.130896372_130896374del
GRCh37.p13 chr 7	NC_000007.13:g.130896373_130896374del
GRCh37.p13 chr 7	NC_000007.13:g.130896374del
GRCh37.p13 chr 7	NC_000007.13:g.130896374dup
GRCh37.p13 chr 7	NC_000007.13:g.130896373_130896374dup

Gene: MKLN1, muskelin 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MKLN1 transcript variant 1	NM_001145354.2:c.29+68672… NM_001145354.2:c.29+68672_29+68674del	N/A	Intron Variant
MKLN1 transcript variant 3	NM_001321316.2:c.	N/A	Genic Upstream Transcript Variant
MKLN1 transcript variant 2	NM_013255.5:c.	N/A	Genic Upstream Transcript Variant
MKLN1 transcript variant X2	XM_047420401.1:c.29+68672… XM_047420401.1:c.29+68672_29+68674del	N/A	Intron Variant
MKLN1 transcript variant X1	XM_006715993.4:c.	N/A	Genic Upstream Transcript Variant
MKLN1 transcript variant X3	XM_011516224.4:c.	N/A	Genic Upstream Transcript Variant
MKLN1 transcript variant X4	XM_047420402.1:c.	N/A	Genic Upstream Transcript Variant

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

Not Reported in ClinVar

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

Placement	(T)₁₃=	delTTT	delTT	delT	dupT	dupTT
GRCh38.p14 chr 7	NC_000007.14:g.131211603_131211615=	NC_000007.14:g.131211613_131211615del	NC_000007.14:g.131211614_131211615del	NC_000007.14:g.131211615del	NC_000007.14:g.131211615dup	NC_000007.14:g.131211614_131211615dup
GRCh37.p13 chr 7	NC_000007.13:g.130896362_130896374=	NC_000007.13:g.130896372_130896374del	NC_000007.13:g.130896373_130896374del	NC_000007.13:g.130896374del	NC_000007.13:g.130896374dup	NC_000007.13:g.130896373_130896374dup
MKLN1 transcript variant 1	NM_001145354.1:c.29+68662=	NM_001145354.1:c.29+68672_29+68674del	NM_001145354.1:c.29+68673_29+68674del	NM_001145354.1:c.29+68674del	NM_001145354.1:c.29+68674dup	NM_001145354.1:c.29+68673_29+68674dup
MKLN1 transcript variant 1	NM_001145354.2:c.29+68662=	NM_001145354.2:c.29+68672_29+68674del	NM_001145354.2:c.29+68673_29+68674del	NM_001145354.2:c.29+68674del	NM_001145354.2:c.29+68674dup	NM_001145354.2:c.29+68673_29+68674dup
MKLN1 transcript variant X2	XM_047420401.1:c.29+68662=	XM_047420401.1:c.29+68672_29+68674del	XM_047420401.1:c.29+68673_29+68674del	XM_047420401.1:c.29+68674del	XM_047420401.1:c.29+68674dup	XM_047420401.1:c.29+68673_29+68674dup

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#.

45 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42919555	Mar 13, 2006 (126)
2	HUMANGENOME_JCVI	ss95475420	Feb 06, 2009 (130)
3	HUMANGENOME_JCVI	ss98214008	Mar 15, 2016 (147)
4	BCMHGSC_JDW	ss103758536	Dec 01, 2009 (131)
5	GMI	ss288873017	May 04, 2012 (138)
6	PJP	ss295356654	May 09, 2011 (134)
7	SSMP	ss663746109	Jan 10, 2018 (151)
8	1000GENOMES	ss1367738478	Jan 10, 2018 (151)
9	1000GENOMES	ss1367738479	Aug 21, 2014 (142)
10	EVA_UK10K_ALSPAC	ss1705833895	Jan 10, 2018 (151)
11	EVA_UK10K_TWINSUK	ss1705834120	Jan 10, 2018 (151)
12	EVA_UK10K_TWINSUK	ss1710352537	Apr 01, 2015 (144)
13	EVA_UK10K_ALSPAC	ss1710352565	Apr 01, 2015 (144)
14	SWEGEN	ss3002056220	Jan 10, 2018 (151)
15	EVA_DECODE	ss3720718946	Jul 13, 2019 (153)
16	EVA_DECODE	ss3720718948	Jul 13, 2019 (153)
17	EVA_DECODE	ss3720718949	Jul 13, 2019 (153)
18	ACPOP	ss3735083338	Jul 13, 2019 (153)
19	ACPOP	ss3735083339	Jul 13, 2019 (153)
20	ACPOP	ss3735083340	Jul 13, 2019 (153)
21	PACBIO	ss3785961776	Jul 13, 2019 (153)
22	PACBIO	ss3791239908	Jul 13, 2019 (153)
23	PACBIO	ss3791239909	Jul 13, 2019 (153)
24	PACBIO	ss3796120067	Jul 13, 2019 (153)
25	PACBIO	ss3796120068	Jul 13, 2019 (153)
26	KHV_HUMAN_GENOMES	ss3810345528	Jul 13, 2019 (153)
27	KHV_HUMAN_GENOMES	ss3810345529	Jul 13, 2019 (153)
28	EVA	ss3830826613	Apr 26, 2020 (154)
29	GNOMAD	ss4173348066	Apr 26, 2021 (155)
30	GNOMAD	ss4173348067	Apr 26, 2021 (155)
31	GNOMAD	ss4173348068	Apr 26, 2021 (155)
32	GNOMAD	ss4173348069	Apr 26, 2021 (155)
33	GNOMAD	ss4173348070	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5185646400	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5185646401	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5185646402	Apr 26, 2021 (155)
37	1000G_HIGH_COVERAGE	ss5274786896	Oct 13, 2022 (156)
38	HUGCELL_USP	ss5471667646	Oct 13, 2022 (156)
39	HUGCELL_USP	ss5471667647	Oct 13, 2022 (156)
40	HUGCELL_USP	ss5471667648	Oct 13, 2022 (156)
41	TOMMO_GENOMICS	ss5726659864	Oct 13, 2022 (156)
42	TOMMO_GENOMICS	ss5726659865	Oct 13, 2022 (156)
43	TOMMO_GENOMICS	ss5726659866	Oct 13, 2022 (156)
44	EVA	ss5823544748	Oct 13, 2022 (156)
45	EVA	ss5823544749	Oct 13, 2022 (156)
46	1000Genomes	NC_000007.13 - 130896362	Oct 12, 2018 (152)
47	The Avon Longitudinal Study of Parents and Children	NC_000007.13 - 130896362	Oct 12, 2018 (152)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277062832 (NC_000007.14:131211602::T 3406/134670) Row 277062833 (NC_000007.14:131211602::TT 6/134754) Row 277062834 (NC_000007.14:131211602:T: 20664/134618)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277062832 (NC_000007.14:131211602::T 3406/134670) Row 277062833 (NC_000007.14:131211602::TT 6/134754) Row 277062834 (NC_000007.14:131211602:T: 20664/134618)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277062832 (NC_000007.14:131211602::T 3406/134670) Row 277062833 (NC_000007.14:131211602::TT 6/134754) Row 277062834 (NC_000007.14:131211602:T: 20664/134618)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277062832 (NC_000007.14:131211602::T 3406/134670) Row 277062833 (NC_000007.14:131211602::TT 6/134754) Row 277062834 (NC_000007.14:131211602:T: 20664/134618)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 277062832 (NC_000007.14:131211602::T 3406/134670) Row 277062833 (NC_000007.14:131211602::TT 6/134754) Row 277062834 (NC_000007.14:131211602:T: 20664/134618)...	-	Apr 26, 2021 (155)
53	Northern Sweden Submission ignored due to conflicting rows: Row 8368203 (NC_000007.13:130896361:T: 99/600) Row 8368204 (NC_000007.13:130896361:TT: 132/600) Row 8368205 (NC_000007.13:130896361::T 2/600)	-	Jul 13, 2019 (153)
54	Northern Sweden Submission ignored due to conflicting rows: Row 8368203 (NC_000007.13:130896361:T: 99/600) Row 8368204 (NC_000007.13:130896361:TT: 132/600) Row 8368205 (NC_000007.13:130896361::T 2/600)	-	Jul 13, 2019 (153)
55	Northern Sweden Submission ignored due to conflicting rows: Row 8368203 (NC_000007.13:130896361:T: 99/600) Row 8368204 (NC_000007.13:130896361:TT: 132/600) Row 8368205 (NC_000007.13:130896361::T 2/600)	-	Jul 13, 2019 (153)
56	8.3KJPN Submission ignored due to conflicting rows: Row 43615707 (NC_000007.13:130896361::T 7/16758) Row 43615708 (NC_000007.13:130896361:TT: 656/16758) Row 43615709 (NC_000007.13:130896361:T: 586/16758)	-	Apr 26, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 43615707 (NC_000007.13:130896361::T 7/16758) Row 43615708 (NC_000007.13:130896361:TT: 656/16758) Row 43615709 (NC_000007.13:130896361:T: 586/16758)	-	Apr 26, 2021 (155)
58	8.3KJPN Submission ignored due to conflicting rows: Row 43615707 (NC_000007.13:130896361::T 7/16758) Row 43615708 (NC_000007.13:130896361:TT: 656/16758) Row 43615709 (NC_000007.13:130896361:T: 586/16758)	-	Apr 26, 2021 (155)
59	14KJPN Submission ignored due to conflicting rows: Row 60496968 (NC_000007.14:131211602:T: 985/28258) Row 60496969 (NC_000007.14:131211602:TT: 1122/28258) Row 60496970 (NC_000007.14:131211602::T 9/28258)	-	Oct 13, 2022 (156)
60	14KJPN Submission ignored due to conflicting rows: Row 60496968 (NC_000007.14:131211602:T: 985/28258) Row 60496969 (NC_000007.14:131211602:TT: 1122/28258) Row 60496970 (NC_000007.14:131211602::T 9/28258)	-	Oct 13, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 60496968 (NC_000007.14:131211602:T: 985/28258) Row 60496969 (NC_000007.14:131211602:TT: 1122/28258) Row 60496970 (NC_000007.14:131211602::T 9/28258)	-	Oct 13, 2022 (156)
62	UK 10K study - Twins	-	Oct 12, 2018 (152)
63	UK 10K study - Twins Submission ignored due to conflicting rows: Row 21830115 (NC_000007.13:130896361:TT: 862/3708) Row 21830116 (NC_000007.13:130896362:T: 513/3708)	-	Apr 26, 2020 (154)
64	ALFA	NC_000007.14 - 131211603	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)
rs68191266	Feb 27, 2009 (130)
rs72061231	Oct 12, 2011 (135)
rs200281791	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4173348070	NC_000007.14:131211602:TTT:	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT:TTTTTTTTTT	(self)
1556224972	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT:TTTTTTTTTT	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT:TTTTTTTTTT	(self)
39234269, 21830115, ss663746109, ss1367738478, ss1705833895, ss1705834120, ss3002056220, ss3735083339, ss3785961776, ss3791239908, ss3796120067, ss5185646401, ss5823544748	NC_000007.13:130896361:TT:	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3720718946, ss3810345528, ss4173348069, ss5471667646, ss5726659865	NC_000007.14:131211602:TT:	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
1556224972	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT:TTTTTTTTTTT	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss95475420, ss98214008, ss103758536	NT_007933.15:68929215:TT:	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss288873017, ss295356654	NC_000007.12:130546901:T:	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3735083338, ss3830826613, ss5185646402, ss5823544749	NC_000007.13:130896361:T:	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss1367738479, ss1710352537, ss1710352565	NC_000007.13:130896362:T:	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4173348068, ss5274786896, ss5471667647, ss5726659864	NC_000007.14:131211602:T:	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
1556224972	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3720718948, ss3810345529	NC_000007.14:131211603:T:	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss42919555	NT_007933.15:68929204:T:	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss98214008	NT_007933.15:68929215:TT:T	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3735083340, ss3791239909, ss3796120068, ss5185646400	NC_000007.13:130896361::T	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4173348066, ss5471667648, ss5726659866	NC_000007.14:131211602::T	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
1556224972	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3720718949	NC_000007.14:131211604::T	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4173348067	NC_000007.14:131211602::TT	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
1556224972	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000007.14:131211602:TTTTTTTTTTT… NC_000007.14:131211602:TTTTTTTTTTTTT: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 rs34469545

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

rs34469545