Name: rs34739007
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.

rs34739007

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:190668624-190668636 (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(A)₄ / delAAA / delAA / delA / …
del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.06383 (691/10825, ALFA)
delA=0.2266 (1135/5008, 1000G)
delA=0.20 (8/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC01720 : 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	10825	AAAAAAAAAAAAA=0.92988	AAAAAAAAAAA=0.00000, AAAAAAAAAAAA=0.06383, AAAAAAAAAAAAAA=0.00600, AAAAAAAAAAAAAAA=0.00028, AAAAAAAAAAAAAAAA=0.00000	0.882276	0.008797	0.108928	19
European	Sub	9485	AAAAAAAAAAAAA=0.9203	AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0725, AAAAAAAAAAAAAA=0.0069, AAAAAAAAAAAAAAA=0.0003, AAAAAAAAAAAAAAAA=0.0000	0.865825	0.009844	0.124331	13
African	Sub	672	AAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	24	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	648	AAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	52	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	42	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	10	AAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	100	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	228	AAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	60	AAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	228	AAAAAAAAAAAAA=0.987	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.013, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000	0.982456	0.008772	0.008772	27

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	10825	(A)₁₃=0.92988	delAA=0.00000, delA=0.06383, dupA=0.00600, dupAA=0.00028, dupAAA=0.00000
Allele Frequency Aggregator	European	Sub	9485	(A)₁₃=0.9203	delAA=0.0000, delA=0.0725, dupA=0.0069, dupAA=0.0003, dupAAA=0.0000
Allele Frequency Aggregator	African	Sub	672	(A)₁₃=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	228	(A)₁₃=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Other	Sub	228	(A)₁₃=0.987	delAA=0.000, delA=0.013, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	100	(A)₁₃=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	South Asian	Sub	60	(A)₁₃=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Asian	Sub	52	(A)₁₃=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
1000Genomes	Global	Study-wide	5008	(A)₁₃=0.7734	delA=0.2266
1000Genomes	African	Sub	1322	(A)₁₃=0.6808	delA=0.3192
1000Genomes	East Asian	Sub	1008	(A)₁₃=0.7302	delA=0.2698
1000Genomes	Europe	Sub	1006	(A)₁₃=0.8499	delA=0.1501
1000Genomes	South Asian	Sub	978	(A)₁₃=0.870	delA=0.130
1000Genomes	American	Sub	694	(A)₁₃=0.765	delA=0.235
The Danish reference pan genome	Danish	Study-wide	40	(A)₁₃=0.80	delA=0.20

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.190668633_190668636del
GRCh38.p14 chr 1	NC_000001.11:g.190668634_190668636del
GRCh38.p14 chr 1	NC_000001.11:g.190668635_190668636del
GRCh38.p14 chr 1	NC_000001.11:g.190668636del
GRCh38.p14 chr 1	NC_000001.11:g.190668636dup
GRCh38.p14 chr 1	NC_000001.11:g.190668635_190668636dup
GRCh38.p14 chr 1	NC_000001.11:g.190668634_190668636dup
GRCh37.p13 chr 1	NC_000001.10:g.190637763_190637766del
GRCh37.p13 chr 1	NC_000001.10:g.190637764_190637766del
GRCh37.p13 chr 1	NC_000001.10:g.190637765_190637766del
GRCh37.p13 chr 1	NC_000001.10:g.190637766del
GRCh37.p13 chr 1	NC_000001.10:g.190637766dup
GRCh37.p13 chr 1	NC_000001.10:g.190637765_190637766dup
GRCh37.p13 chr 1	NC_000001.10:g.190637764_190637766dup

Gene: LINC01720, long intergenic non-protein coding RNA 1720 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC01720 transcript	NR_033922.2:n.	N/A	Intron 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	(A)₁₃=	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA
GRCh38.p14 chr 1	NC_000001.11:g.190668624_190668636=	NC_000001.11:g.190668633_190668636del	NC_000001.11:g.190668634_190668636del	NC_000001.11:g.190668635_190668636del	NC_000001.11:g.190668636del	NC_000001.11:g.190668636dup	NC_000001.11:g.190668635_190668636dup	NC_000001.11:g.190668634_190668636dup
GRCh37.p13 chr 1	NC_000001.10:g.190637754_190637766=	NC_000001.10:g.190637763_190637766del	NC_000001.10:g.190637764_190637766del	NC_000001.10:g.190637765_190637766del	NC_000001.10:g.190637766del	NC_000001.10:g.190637766dup	NC_000001.10:g.190637765_190637766dup	NC_000001.10:g.190637764_190637766dup

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#.

47 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41155051	Dec 03, 2013 (138)
2	BCMHGSC_JDW	ss103495238	Dec 01, 2009 (131)
3	GMI	ss288070245	May 04, 2012 (137)
4	SSMP	ss663142478	Apr 01, 2015 (144)
5	1000GENOMES	ss1367935927	Aug 21, 2014 (142)
6	EVA_GENOME_DK	ss1574067929	Apr 01, 2015 (144)
7	SWEGEN	ss2988154558	Nov 08, 2017 (151)
8	MCHAISSO	ss3065341158	Nov 08, 2017 (151)
9	BEROUKHIMLAB	ss3644074694	Oct 11, 2018 (152)
10	EVA_DECODE	ss3688270109	Jul 12, 2019 (153)
11	EVA_DECODE	ss3688270110	Jul 12, 2019 (153)
12	EVA_DECODE	ss3688270111	Jul 12, 2019 (153)
13	EVA_DECODE	ss3688270112	Jul 12, 2019 (153)
14	ACPOP	ss3727702379	Jul 12, 2019 (153)
15	ACPOP	ss3727702380	Jul 12, 2019 (153)
16	KHV_HUMAN_GENOMES	ss3800118088	Jul 12, 2019 (153)
17	EVA	ss3826553490	Apr 25, 2020 (154)
18	EVA	ss3836674187	Apr 25, 2020 (154)
19	EVA	ss3842084867	Apr 25, 2020 (154)
20	KOGIC	ss3946137328	Apr 25, 2020 (154)
21	KOGIC	ss3946137329	Apr 25, 2020 (154)
22	KOGIC	ss3946137330	Apr 25, 2020 (154)
23	KOGIC	ss3946137331	Apr 25, 2020 (154)
24	GNOMAD	ss4008076173	Apr 25, 2021 (155)
25	GNOMAD	ss4008076174	Apr 25, 2021 (155)
26	GNOMAD	ss4008076175	Apr 25, 2021 (155)
27	GNOMAD	ss4008076176	Apr 25, 2021 (155)
28	GNOMAD	ss4008076177	Apr 25, 2021 (155)
29	GNOMAD	ss4008076178	Apr 25, 2021 (155)
30	TOMMO_GENOMICS	ss5147609718	Apr 25, 2021 (155)
31	TOMMO_GENOMICS	ss5147609719	Apr 25, 2021 (155)
32	TOMMO_GENOMICS	ss5147609720	Apr 25, 2021 (155)
33	TOMMO_GENOMICS	ss5147609721	Apr 25, 2021 (155)
34	1000G_HIGH_COVERAGE	ss5245164353	Oct 12, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5245164354	Oct 12, 2022 (156)
36	HUGCELL_USP	ss5445662767	Oct 12, 2022 (156)
37	HUGCELL_USP	ss5445662768	Oct 12, 2022 (156)
38	HUGCELL_USP	ss5445662769	Oct 12, 2022 (156)
39	HUGCELL_USP	ss5445662770	Oct 12, 2022 (156)
40	HUGCELL_USP	ss5445662771	Oct 12, 2022 (156)
41	EVA	ss5506122843	Oct 12, 2022 (156)
42	TOMMO_GENOMICS	ss5675131950	Oct 12, 2022 (156)
43	TOMMO_GENOMICS	ss5675131951	Oct 12, 2022 (156)
44	TOMMO_GENOMICS	ss5675131952	Oct 12, 2022 (156)
45	TOMMO_GENOMICS	ss5675131953	Oct 12, 2022 (156)
46	EVA	ss5833008410	Oct 12, 2022 (156)
47	EVA	ss5849208977	Oct 12, 2022 (156)
48	1000Genomes	NC_000001.10 - 190637754	Oct 11, 2018 (152)
49	The Danish reference pan genome	NC_000001.10 - 190637754	Apr 25, 2020 (154)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 34298909 (NC_000001.11:190668623::A 3463/129124) Row 34298910 (NC_000001.11:190668623::AA 1026/129226) Row 34298911 (NC_000001.11:190668623::AAA 1/129240)...	-	Apr 25, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 34298909 (NC_000001.11:190668623::A 3463/129124) Row 34298910 (NC_000001.11:190668623::AA 1026/129226) Row 34298911 (NC_000001.11:190668623::AAA 1/129240)...	-	Apr 25, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 34298909 (NC_000001.11:190668623::A 3463/129124) Row 34298910 (NC_000001.11:190668623::AA 1026/129226) Row 34298911 (NC_000001.11:190668623::AAA 1/129240)...	-	Apr 25, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 34298909 (NC_000001.11:190668623::A 3463/129124) Row 34298910 (NC_000001.11:190668623::AA 1026/129226) Row 34298911 (NC_000001.11:190668623::AAA 1/129240)...	-	Apr 25, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 34298909 (NC_000001.11:190668623::A 3463/129124) Row 34298910 (NC_000001.11:190668623::AA 1026/129226) Row 34298911 (NC_000001.11:190668623::AAA 1/129240)...	-	Apr 25, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 34298909 (NC_000001.11:190668623::A 3463/129124) Row 34298910 (NC_000001.11:190668623::AA 1026/129226) Row 34298911 (NC_000001.11:190668623::AAA 1/129240)...	-	Apr 25, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 34298909 (NC_000001.11:190668623::A 3463/129124) Row 34298910 (NC_000001.11:190668623::AA 1026/129226) Row 34298911 (NC_000001.11:190668623::AAA 1/129240)...	-	Apr 25, 2021 (155)
57	Korean Genome Project Submission ignored due to conflicting rows: Row 2515329 (NC_000001.11:190668626::A 83/1832) Row 2515330 (NC_000001.11:190668625:A: 441/1832) Row 2515331 (NC_000001.11:190668624:AA: 4/1832)...	-	Apr 25, 2020 (154)
58	Korean Genome Project Submission ignored due to conflicting rows: Row 2515329 (NC_000001.11:190668626::A 83/1832) Row 2515330 (NC_000001.11:190668625:A: 441/1832) Row 2515331 (NC_000001.11:190668624:AA: 4/1832)...	-	Apr 25, 2020 (154)
59	Korean Genome Project Submission ignored due to conflicting rows: Row 2515329 (NC_000001.11:190668626::A 83/1832) Row 2515330 (NC_000001.11:190668625:A: 441/1832) Row 2515331 (NC_000001.11:190668624:AA: 4/1832)...	-	Apr 25, 2020 (154)
60	Korean Genome Project Submission ignored due to conflicting rows: Row 2515329 (NC_000001.11:190668626::A 83/1832) Row 2515330 (NC_000001.11:190668625:A: 441/1832) Row 2515331 (NC_000001.11:190668624:AA: 4/1832)...	-	Apr 25, 2020 (154)
61	Northern Sweden Submission ignored due to conflicting rows: Row 987244 (NC_000001.10:190637753:A: 91/600) Row 987245 (NC_000001.10:190637753::A 4/600)	-	Jul 12, 2019 (153)
62	Northern Sweden Submission ignored due to conflicting rows: Row 987244 (NC_000001.10:190637753:A: 91/600) Row 987245 (NC_000001.10:190637753::A 4/600)	-	Jul 12, 2019 (153)
63	8.3KJPN Submission ignored due to conflicting rows: Row 5579025 (NC_000001.10:190637753:A: 3700/16760) Row 5579026 (NC_000001.10:190637753::A 351/16760) Row 5579027 (NC_000001.10:190637753:AAA: 92/16760)...	-	Apr 25, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 5579025 (NC_000001.10:190637753:A: 3700/16760) Row 5579026 (NC_000001.10:190637753::A 351/16760) Row 5579027 (NC_000001.10:190637753:AAA: 92/16760)...	-	Apr 25, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 5579025 (NC_000001.10:190637753:A: 3700/16760) Row 5579026 (NC_000001.10:190637753::A 351/16760) Row 5579027 (NC_000001.10:190637753:AAA: 92/16760)...	-	Apr 25, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 5579025 (NC_000001.10:190637753:A: 3700/16760) Row 5579026 (NC_000001.10:190637753::A 351/16760) Row 5579027 (NC_000001.10:190637753:AAA: 92/16760)...	-	Apr 25, 2021 (155)
67	14KJPN Submission ignored due to conflicting rows: Row 8969054 (NC_000001.11:190668623::A 567/28256) Row 8969055 (NC_000001.11:190668623:A: 6340/28256) Row 8969056 (NC_000001.11:190668623:AAA: 165/28256)...	-	Oct 12, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 8969054 (NC_000001.11:190668623::A 567/28256) Row 8969055 (NC_000001.11:190668623:A: 6340/28256) Row 8969056 (NC_000001.11:190668623:AAA: 165/28256)...	-	Oct 12, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 8969054 (NC_000001.11:190668623::A 567/28256) Row 8969055 (NC_000001.11:190668623:A: 6340/28256) Row 8969056 (NC_000001.11:190668623:AAA: 165/28256)...	-	Oct 12, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 8969054 (NC_000001.11:190668623::A 567/28256) Row 8969055 (NC_000001.11:190668623:A: 6340/28256) Row 8969056 (NC_000001.11:190668623:AAA: 165/28256)...	-	Oct 12, 2022 (156)
71	ALFA	NC_000001.11 - 190668624	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)
rs66492626	May 11, 2012 (137)
rs71709424	May 11, 2012 (137)
rs199868282	May 11, 2012 (137)
rs374688938	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4008076178, ss5445662771	NC_000001.11:190668623:AAAA:	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAA	(self)
ss5147609720	NC_000001.10:190637753:AAA:	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss3946137331, ss4008076177, ss5675131952	NC_000001.11:190668623:AAA:	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss5147609721	NC_000001.10:190637753:AA:	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3065341158, ss3688270112, ss4008076176, ss5445662769, ss5675131953	NC_000001.11:190668623:AA:	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAA	(self)
13348353203	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAA	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss3946137330	NC_000001.11:190668624:AA:	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss103495238	NT_004487.19:42126406:AA:	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss288070245	NC_000001.9:188904376:A:	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
4756776, 188740, ss663142478, ss1367935927, ss1574067929, ss2988154558, ss3644074694, ss3727702379, ss3826553490, ss3836674187, ss5147609718, ss5833008410	NC_000001.10:190637753:A:	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3800118088, ss3842084867, ss5245164353, ss5445662767, ss5675131951, ss5849208977	NC_000001.11:190668623:A:	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
13348353203	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3688270111	NC_000001.11:190668624:A:	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3946137329	NC_000001.11:190668625:A:	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss41155051	NT_004487.19:42126396:A:	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3727702380, ss5147609719, ss5506122843	NC_000001.10:190637753::A	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4008076173, ss5245164354, ss5445662768, ss5675131950	NC_000001.11:190668623::A	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
13348353203	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3688270110	NC_000001.11:190668625::A	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3946137328	NC_000001.11:190668626::A	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4008076174, ss5445662770	NC_000001.11:190668623::AA	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
13348353203	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3688270109	NC_000001.11:190668625::AA	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4008076175	NC_000001.11:190668623::AAA	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
13348353203	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000001.11:190668623:AAAAAAAAAAA… NC_000001.11:190668623:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(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 rs34739007

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

rs34739007