Name: rs34215474
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.

rs34215474

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr18:12347555-12347568 (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 / dup(T)₁₁
Variation Type: Indel Insertion and Deletion
Frequency: (T)₁₄=0.2188 (1096/5008, 1000G)
del(T)₄=0.000 (0/948, ALFA)
delTT=0.000 (0/948, ALFA) (+ 4 more)
delT=0.000 (0/948, ALFA)
dupT=0.000 (0/948, ALFA)
dupTT=0.000 (0/948, ALFA)
(T)₁₄=0.25 (10/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: AFG3L2 : 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	HWEP
Total	Global	948	TTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000	1.0	N/A
European	Sub	392	TTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000	1.0	N/A
African	Sub	378	TTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000	1.0	N/A
African Others	Sub	20	TTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	358	TTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000	1.0	N/A
Asian	Sub	20	TTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	16	TTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	4	TTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0	1.0	N/A
Latin American 1	Sub	12	TTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 2	Sub	96	TTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	N/A
South Asian	Sub	4	TTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0	1.0	N/A
Other	Sub	46	TTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	(T)₁₄=0.2188	delT=0.7812
1000Genomes	African	Sub	1322	(T)₁₄=0.3986	delT=0.6014
1000Genomes	East Asian	Sub	1008	(T)₁₄=0.1538	delT=0.8462
1000Genomes	Europe	Sub	1006	(T)₁₄=0.1451	delT=0.8549
1000Genomes	South Asian	Sub	978	(T)₁₄=0.138	delT=0.862
1000Genomes	American	Sub	694	(T)₁₄=0.192	delT=0.808
Allele Frequency Aggregator	Total	Global	948	(T)₁₄=1.000	del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	European	Sub	392	(T)₁₄=1.000	del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	African	Sub	378	(T)₁₄=1.000	del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	96	(T)₁₄=1.00	del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Other	Sub	46	(T)₁₄=1.00	del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Asian	Sub	20	(T)₁₄=1.00	del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Latin American 1	Sub	12	(T)₁₄=1.00	del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	South Asian	Sub	4	(T)₁₄=1.0	del(T)₄=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0
The Danish reference pan genome	Danish	Study-wide	40	(T)₁₄=0.25	delT=0.75

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 18	NC_000018.10:g.12347565_12347568del
GRCh38.p14 chr 18	NC_000018.10:g.12347566_12347568del
GRCh38.p14 chr 18	NC_000018.10:g.12347567_12347568del
GRCh38.p14 chr 18	NC_000018.10:g.12347568del
GRCh38.p14 chr 18	NC_000018.10:g.12347568dup
GRCh38.p14 chr 18	NC_000018.10:g.12347567_12347568dup
GRCh38.p14 chr 18	NC_000018.10:g.12347558_12347568dup
GRCh37.p13 chr 18	NC_000018.9:g.12347564_12347567del
GRCh37.p13 chr 18	NC_000018.9:g.12347565_12347567del
GRCh37.p13 chr 18	NC_000018.9:g.12347566_12347567del
GRCh37.p13 chr 18	NC_000018.9:g.12347567del
GRCh37.p13 chr 18	NC_000018.9:g.12347567dup
GRCh37.p13 chr 18	NC_000018.9:g.12347566_12347567dup
GRCh37.p13 chr 18	NC_000018.9:g.12347557_12347567dup
AFG3L2 RefSeqGene (LRG_666)	NG_023361.1:g.34719_34722del
AFG3L2 RefSeqGene (LRG_666)	NG_023361.1:g.34720_34722del
AFG3L2 RefSeqGene (LRG_666)	NG_023361.1:g.34721_34722del
AFG3L2 RefSeqGene (LRG_666)	NG_023361.1:g.34722del
AFG3L2 RefSeqGene (LRG_666)	NG_023361.1:g.34722dup
AFG3L2 RefSeqGene (LRG_666)	NG_023361.1:g.34721_34722dup
AFG3L2 RefSeqGene (LRG_666)	NG_023361.1:g.34712_34722dup

Gene: AFG3L2, AFG3 like matrix AAA peptidase subunit 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
AFG3L2 transcript	NM_006796.3:c.1663+715_16… NM_006796.3:c.1663+715_1663+718del	N/A	Intron Variant
AFG3L2 transcript variant X1	XM_011525601.4:c.1663+715… XM_011525601.4:c.1663+715_1663+718del	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	(T)₁₄=	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dup(T)₁₁
GRCh38.p14 chr 18	NC_000018.10:g.12347555_12347568=	NC_000018.10:g.12347565_12347568del	NC_000018.10:g.12347566_12347568del	NC_000018.10:g.12347567_12347568del	NC_000018.10:g.12347568del	NC_000018.10:g.12347568dup	NC_000018.10:g.12347567_12347568dup	NC_000018.10:g.12347558_12347568dup
GRCh37.p13 chr 18	NC_000018.9:g.12347554_12347567=	NC_000018.9:g.12347564_12347567del	NC_000018.9:g.12347565_12347567del	NC_000018.9:g.12347566_12347567del	NC_000018.9:g.12347567del	NC_000018.9:g.12347567dup	NC_000018.9:g.12347566_12347567dup	NC_000018.9:g.12347557_12347567dup
AFG3L2 RefSeqGene (LRG_666)	NG_023361.1:g.34709_34722=	NG_023361.1:g.34719_34722del	NG_023361.1:g.34720_34722del	NG_023361.1:g.34721_34722del	NG_023361.1:g.34722del	NG_023361.1:g.34722dup	NG_023361.1:g.34721_34722dup	NG_023361.1:g.34712_34722dup
AFG3L2 transcript	NM_006796.2:c.1663+718=	NM_006796.2:c.1663+715_1663+718del	NM_006796.2:c.1663+716_1663+718del	NM_006796.2:c.1663+717_1663+718del	NM_006796.2:c.1663+718del	NM_006796.2:c.1663+718dup	NM_006796.2:c.1663+717_1663+718dup	NM_006796.2:c.1663+708_1663+718dup
AFG3L2 transcript	NM_006796.3:c.1663+718=	NM_006796.3:c.1663+715_1663+718del	NM_006796.3:c.1663+716_1663+718del	NM_006796.3:c.1663+717_1663+718del	NM_006796.3:c.1663+718del	NM_006796.3:c.1663+718dup	NM_006796.3:c.1663+717_1663+718dup	NM_006796.3:c.1663+708_1663+718dup
AFG3L2 transcript variant X1	XM_011525601.4:c.1663+718=	XM_011525601.4:c.1663+715_1663+718del	XM_011525601.4:c.1663+716_1663+718del	XM_011525601.4:c.1663+717_1663+718del	XM_011525601.4:c.1663+718del	XM_011525601.4:c.1663+718dup	XM_011525601.4:c.1663+717_1663+718dup	XM_011525601.4:c.1663+708_1663+718dup

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#.

49 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40946924	Mar 13, 2006 (126)
2	HUMANGENOME_JCVI	ss95705743	Feb 04, 2009 (130)
3	HUMANGENOME_JCVI	ss96363302	Feb 04, 2009 (130)
4	BUSHMAN	ss193470321	Jul 04, 2010 (137)
5	BL	ss256191940	May 09, 2011 (137)
6	GMI	ss289347985	May 04, 2012 (137)
7	SSMP	ss664384705	Apr 01, 2015 (144)
8	BILGI_BIOE	ss666705003	Apr 25, 2013 (138)
9	1000GENOMES	ss1377201792	Aug 21, 2014 (142)
10	DDI	ss1536862166	Apr 01, 2015 (144)
11	EVA_GENOME_DK	ss1575118768	Apr 01, 2015 (144)
12	JJLAB	ss2031359963	Sep 14, 2016 (149)
13	MCHAISSO	ss3063884476	Nov 08, 2017 (151)
14	MCHAISSO	ss3064728941	Nov 08, 2017 (151)
15	BIOINF_KMB_FNS_UNIBA	ss3645475992	Oct 12, 2018 (152)
16	URBANLAB	ss3650744238	Oct 12, 2018 (152)
17	EVA_DECODE	ss3701247597	Jul 13, 2019 (153)
18	EVA_DECODE	ss3701247599	Jul 13, 2019 (153)
19	EVA_DECODE	ss3701247600	Jul 13, 2019 (153)
20	EVA_DECODE	ss3701247601	Jul 13, 2019 (153)
21	EVA_DECODE	ss3701247602	Jul 13, 2019 (153)
22	ACPOP	ss3742366528	Jul 13, 2019 (153)
23	ACPOP	ss3742366530	Jul 13, 2019 (153)
24	PACBIO	ss3788317549	Jul 13, 2019 (153)
25	PACBIO	ss3793257325	Jul 13, 2019 (153)
26	PACBIO	ss3798143553	Jul 13, 2019 (153)
27	KHV_HUMAN_GENOMES	ss3820403803	Jul 13, 2019 (153)
28	EVA	ss3835068610	Apr 27, 2020 (154)
29	KOGIC	ss3979634653	Apr 27, 2020 (154)
30	KOGIC	ss3979634654	Apr 27, 2020 (154)
31	GNOMAD	ss4318346756	Apr 26, 2021 (155)
32	GNOMAD	ss4318346757	Apr 26, 2021 (155)
33	GNOMAD	ss4318346760	Apr 26, 2021 (155)
34	GNOMAD	ss4318346761	Apr 26, 2021 (155)
35	GNOMAD	ss4318346762	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5224226130	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5224226131	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5224226132	Apr 26, 2021 (155)
39	1000G_HIGH_COVERAGE	ss5304521850	Oct 16, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5304521851	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5497417973	Oct 16, 2022 (156)
42	HUGCELL_USP	ss5497417974	Oct 16, 2022 (156)
43	HUGCELL_USP	ss5497417975	Oct 16, 2022 (156)
44	EVA	ss5511866125	Oct 16, 2022 (156)
45	TOMMO_GENOMICS	ss5781012843	Oct 16, 2022 (156)
46	TOMMO_GENOMICS	ss5781012845	Oct 16, 2022 (156)
47	TOMMO_GENOMICS	ss5781012846	Oct 16, 2022 (156)
48	EVA	ss5827260319	Oct 16, 2022 (156)
49	EVA	ss5873253200	Oct 16, 2022 (156)
50	1000Genomes	NC_000018.9 - 12347554	Oct 12, 2018 (152)
51	The Danish reference pan genome	NC_000018.9 - 12347554	Apr 27, 2020 (154)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518379674 (NC_000018.10:12347554::T 3422/129490) Row 518379675 (NC_000018.10:12347554::TT 7/129538) Row 518379678 (NC_000018.10:12347554:T: 93976/129460)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518379674 (NC_000018.10:12347554::T 3422/129490) Row 518379675 (NC_000018.10:12347554::TT 7/129538) Row 518379678 (NC_000018.10:12347554:T: 93976/129460)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518379674 (NC_000018.10:12347554::T 3422/129490) Row 518379675 (NC_000018.10:12347554::TT 7/129538) Row 518379678 (NC_000018.10:12347554:T: 93976/129460)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518379674 (NC_000018.10:12347554::T 3422/129490) Row 518379675 (NC_000018.10:12347554::TT 7/129538) Row 518379678 (NC_000018.10:12347554:T: 93976/129460)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518379674 (NC_000018.10:12347554::T 3422/129490) Row 518379675 (NC_000018.10:12347554::TT 7/129538) Row 518379678 (NC_000018.10:12347554:T: 93976/129460)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518379674 (NC_000018.10:12347554::T 3422/129490) Row 518379675 (NC_000018.10:12347554::TT 7/129538) Row 518379678 (NC_000018.10:12347554:T: 93976/129460)...	-	Apr 26, 2021 (155)
58	Korean Genome Project Submission ignored due to conflicting rows: Row 36012654 (NC_000018.10:12347556:T: 999/1826) Row 36012655 (NC_000018.10:12347555:TT: 13/1826)	-	Apr 27, 2020 (154)
59	Korean Genome Project Submission ignored due to conflicting rows: Row 36012654 (NC_000018.10:12347556:T: 999/1826) Row 36012655 (NC_000018.10:12347555:TT: 13/1826)	-	Apr 27, 2020 (154)
60	Northern Sweden Submission ignored due to conflicting rows: Row 15651393 (NC_000018.9:12347553:T: 430/576) Row 15651395 (NC_000018.9:12347553:TT: 1/576)	-	Jul 13, 2019 (153)
61	Northern Sweden Submission ignored due to conflicting rows: Row 15651393 (NC_000018.9:12347553:T: 430/576) Row 15651395 (NC_000018.9:12347553:TT: 1/576)	-	Jul 13, 2019 (153)
62	8.3KJPN Submission ignored due to conflicting rows: Row 82195437 (NC_000018.9:12347553:T: 9763/16758) Row 82195438 (NC_000018.9:12347553:TT: 22/16758) Row 82195439 (NC_000018.9:12347553::T 3/16758)	-	Apr 26, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 82195437 (NC_000018.9:12347553:T: 9763/16758) Row 82195438 (NC_000018.9:12347553:TT: 22/16758) Row 82195439 (NC_000018.9:12347553::T 3/16758)	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 82195437 (NC_000018.9:12347553:T: 9763/16758) Row 82195438 (NC_000018.9:12347553:TT: 22/16758) Row 82195439 (NC_000018.9:12347553::T 3/16758)	-	Apr 26, 2021 (155)
65	14KJPN Submission ignored due to conflicting rows: Row 114849947 (NC_000018.10:12347554:T: 16569/28250) Row 114849949 (NC_000018.10:12347554:TT: 29/28250) Row 114849950 (NC_000018.10:12347554::T 4/28250)	-	Oct 16, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 114849947 (NC_000018.10:12347554:T: 16569/28250) Row 114849949 (NC_000018.10:12347554:TT: 29/28250) Row 114849950 (NC_000018.10:12347554::T 4/28250)	-	Oct 16, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 114849947 (NC_000018.10:12347554:T: 16569/28250) Row 114849949 (NC_000018.10:12347554:TT: 29/28250) Row 114849950 (NC_000018.10:12347554::T 4/28250)	-	Oct 16, 2022 (156)
68	ALFA	NC_000018.10 - 12347555	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)
rs113211872	May 11, 2012 (137)
rs150599586	May 04, 2012 (137)
rs376589096	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4318346762	NC_000018.10:12347554:TTTT:	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTT	(self)
12732476665	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTT	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4318346761	NC_000018.10:12347554:TTT:	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3742366530, ss5224226131	NC_000018.9:12347553:TT:	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3701247597, ss4318346760, ss5497417973, ss5781012845	NC_000018.10:12347554:TT:	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
12732476665	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3979634654	NC_000018.10:12347555:TT:	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss256191940, ss289347985	NC_000018.8:12337553:T:	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
73486317, 585934, ss664384705, ss666705003, ss1377201792, ss1536862166, ss1575118768, ss2031359963, ss3742366528, ss3788317549, ss3793257325, ss3798143553, ss3835068610, ss5224226130, ss5511866125, ss5827260319	NC_000018.9:12347553:T:	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3063884476, ss3064728941, ss3645475992, ss3650744238, ss3820403803, ss5304521850, ss5497417974, ss5781012843, ss5873253200	NC_000018.10:12347554:T:	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
12732476665	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3701247599	NC_000018.10:12347555:T:	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3979634653	NC_000018.10:12347556:T:	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss40946924, ss95705743, ss96363302	NT_010859.14:12337566:T:	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss193470321	NT_010859.15:12337554:T:	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss5224226132	NC_000018.9:12347553::T	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4318346756, ss5304521851, ss5497417975, ss5781012846	NC_000018.10:12347554::T	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
12732476665	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3701247600	NC_000018.10:12347556::T	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4318346757	NC_000018.10:12347554::TT	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
12732476665	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3701247601	NC_000018.10:12347556::TT	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3701247602	NC_000018.10:12347556::TTTTTTTTTTT	NC_000018.10:12347554:TTTTTTTTTTTT… NC_000018.10:12347554:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs34215474

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

rs34215474