Name: rs36001734
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.

rs36001734

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:86611011-86611026 (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: delAAA / delAA / delA / dupA / dup…
delAAA / delAA / delA / dupA / dupAA / dupAAA
Variation Type: Indel Insertion and Deletion
Frequency: dupA=0.3055 (2151/7040, ALFA)
dupA=0.4960 (2484/5008, 1000G)
dupA=0.457 (268/586, NorthernSweden) (+ 1 more)
dupA=0.38 (15/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RNF103 : Intron Variant
CHMP3-AS1 : Intron Variant
RNF103-CHMP3 : 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	7040	AAAAAAAAAAAAAAAA=0.6940	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0001, AAAAAAAAAAAAAAAAA=0.3055, AAAAAAAAAAAAAAAAAA=0.0003, AAAAAAAAAAAAAAAAAAA=0.0000	0.563548	0.174296	0.262155	32
European	Sub	6098	AAAAAAAAAAAAAAAA=0.6476	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0002, AAAAAAAAAAAAAAAAA=0.3519, AAAAAAAAAAAAAAAAAA=0.0003, AAAAAAAAAAAAAAAAAAA=0.0000	0.497045	0.200591	0.302364	32
African	Sub	628	AAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	24	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	604	AAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	8	AAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	8	AAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	42	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	134	AAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	30	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	100	AAAAAAAAAAAAAAAA=0.95	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.05, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	0.94	0.04	0.02	17

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	7040	(A)₁₆=0.6940	delAAA=0.0000, delAA=0.0000, delA=0.0001, dupA=0.3055, dupAA=0.0003, dupAAA=0.0000
Allele Frequency Aggregator	European	Sub	6098	(A)₁₆=0.6476	delAAA=0.0000, delAA=0.0000, delA=0.0002, dupA=0.3519, dupAA=0.0003, dupAAA=0.0000
Allele Frequency Aggregator	African	Sub	628	(A)₁₆=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	134	(A)₁₆=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Other	Sub	100	(A)₁₆=0.95	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.05, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	42	(A)₁₆=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	South Asian	Sub	30	(A)₁₆=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Asian	Sub	8	(A)₁₆=1.0	delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupA=0.4960
1000Genomes	African	Sub	1322	- No frequency provided	dupA=0.4153
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupA=0.6597
1000Genomes	Europe	Sub	1006	- No frequency provided	dupA=0.4732
1000Genomes	South Asian	Sub	978	- No frequency provided	dupA=0.484
1000Genomes	American	Sub	694	- No frequency provided	dupA=0.463
Northern Sweden	ACPOP	Study-wide	586	- No frequency provided	dupA=0.457
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupA=0.38

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 2	NC_000002.12:g.86611024_86611026del
GRCh38.p14 chr 2	NC_000002.12:g.86611025_86611026del
GRCh38.p14 chr 2	NC_000002.12:g.86611026del
GRCh38.p14 chr 2	NC_000002.12:g.86611026dup
GRCh38.p14 chr 2	NC_000002.12:g.86611025_86611026dup
GRCh38.p14 chr 2	NC_000002.12:g.86611024_86611026dup
GRCh37.p13 chr 2	NC_000002.11:g.86838147_86838149del
GRCh37.p13 chr 2	NC_000002.11:g.86838148_86838149del
GRCh37.p13 chr 2	NC_000002.11:g.86838149del
GRCh37.p13 chr 2	NC_000002.11:g.86838149dup
GRCh37.p13 chr 2	NC_000002.11:g.86838148_86838149dup
GRCh37.p13 chr 2	NC_000002.11:g.86838147_86838149dup

Gene: RNF103, ring finger protein 103 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RNF103 transcript variant 2	NM_001198951.1:c.470+1146… NM_001198951.1:c.470+1146_470+1148del	N/A	Intron Variant
RNF103 transcript variant 1	NM_005667.4:c.482+1146_48… NM_005667.4:c.482+1146_482+1148del	N/A	Intron Variant
RNF103 transcript variant 3	NM_001198952.2:c.	N/A	Genic Downstream Transcript Variant

Gene: RNF103-CHMP3, RNF103-CHMP3 readthrough (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RNF103-CHMP3 transcript	NM_001198954.1:c.132+9317… NM_001198954.1:c.132+9317_132+9319del	N/A	Intron Variant

Gene: CHMP3-AS1, uncharacterized CHMP3-AS1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CHMP3-AS1 transcript variant X1	XR_940320.4: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)₁₆=	delAAA	delAA	delA	dupA	dupAA	dupAAA
GRCh38.p14 chr 2	NC_000002.12:g.86611011_86611026=	NC_000002.12:g.86611024_86611026del	NC_000002.12:g.86611025_86611026del	NC_000002.12:g.86611026del	NC_000002.12:g.86611026dup	NC_000002.12:g.86611025_86611026dup	NC_000002.12:g.86611024_86611026dup
GRCh37.p13 chr 2	NC_000002.11:g.86838134_86838149=	NC_000002.11:g.86838147_86838149del	NC_000002.11:g.86838148_86838149del	NC_000002.11:g.86838149del	NC_000002.11:g.86838149dup	NC_000002.11:g.86838148_86838149dup	NC_000002.11:g.86838147_86838149dup
RNF103 transcript variant 2	NM_001198951.1:c.470+1148=	NM_001198951.1:c.470+1146_470+1148del	NM_001198951.1:c.470+1147_470+1148del	NM_001198951.1:c.470+1148del	NM_001198951.1:c.470+1148dup	NM_001198951.1:c.470+1147_470+1148dup	NM_001198951.1:c.470+1146_470+1148dup
RNF103-CHMP3 transcript	NM_001198954.1:c.132+9319=	NM_001198954.1:c.132+9317_132+9319del	NM_001198954.1:c.132+9318_132+9319del	NM_001198954.1:c.132+9319del	NM_001198954.1:c.132+9319dup	NM_001198954.1:c.132+9318_132+9319dup	NM_001198954.1:c.132+9317_132+9319dup
RNF103 transcript variant 1	NM_005667.3:c.482+1148=	NM_005667.3:c.482+1146_482+1148del	NM_005667.3:c.482+1147_482+1148del	NM_005667.3:c.482+1148del	NM_005667.3:c.482+1148dup	NM_005667.3:c.482+1147_482+1148dup	NM_005667.3:c.482+1146_482+1148dup
RNF103 transcript variant 1	NM_005667.4:c.482+1148=	NM_005667.4:c.482+1146_482+1148del	NM_005667.4:c.482+1147_482+1148del	NM_005667.4:c.482+1148del	NM_005667.4:c.482+1148dup	NM_005667.4:c.482+1147_482+1148dup	NM_005667.4:c.482+1146_482+1148dup

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#.

44 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41683565	Dec 03, 2013 (138)
2	HUMANGENOME_JCVI	ss95278769	Dec 05, 2013 (138)
3	GMI	ss288190135	May 04, 2012 (137)
4	PJP	ss294993143	May 09, 2011 (137)
5	PJP	ss294993144	May 09, 2011 (135)
6	SSMP	ss663333264	Apr 01, 2015 (144)
7	1000GENOMES	ss1368460562	Aug 21, 2014 (142)
8	EVA_GENOME_DK	ss1575453627	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1702842051	Apr 01, 2015 (144)
10	EVA_UK10K_ALSPAC	ss1702842055	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1702842061	Apr 01, 2015 (144)
12	EVA_UK10K_TWINSUK	ss1702842065	Apr 01, 2015 (144)
13	JJLAB	ss2030427509	Sep 14, 2016 (149)
14	SWEGEN	ss2989897578	Nov 08, 2017 (151)
15	SWEGEN	ss2989897579	Nov 08, 2017 (151)
16	URBANLAB	ss3647081760	Oct 11, 2018 (152)
17	EVA_DECODE	ss3704371148	Jul 13, 2019 (153)
18	EVA_DECODE	ss3704371149	Jul 13, 2019 (153)
19	EVA_DECODE	ss3704371150	Jul 13, 2019 (153)
20	ACPOP	ss3728641850	Jul 13, 2019 (153)
21	KHV_HUMAN_GENOMES	ss3801429414	Jul 13, 2019 (153)
22	EVA	ss3827101229	Apr 25, 2020 (154)
23	GNOMAD	ss4045629269	Apr 26, 2021 (155)
24	GNOMAD	ss4045629270	Apr 26, 2021 (155)
25	GNOMAD	ss4045629271	Apr 26, 2021 (155)
26	GNOMAD	ss4045629272	Apr 26, 2021 (155)
27	GNOMAD	ss4045629273	Apr 26, 2021 (155)
28	GNOMAD	ss4045629274	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5152474299	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5152474300	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5152474301	Apr 26, 2021 (155)
32	1000G_HIGH_COVERAGE	ss5248918653	Oct 12, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5248918654	Oct 12, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5248918655	Oct 12, 2022 (156)
35	HUGCELL_USP	ss5449037867	Oct 12, 2022 (156)
36	HUGCELL_USP	ss5449037868	Oct 12, 2022 (156)
37	HUGCELL_USP	ss5449037869	Oct 12, 2022 (156)
38	TOMMO_GENOMICS	ss5681414584	Oct 12, 2022 (156)
39	TOMMO_GENOMICS	ss5681414585	Oct 12, 2022 (156)
40	TOMMO_GENOMICS	ss5681414586	Oct 12, 2022 (156)
41	EVA	ss5820424914	Oct 12, 2022 (156)
42	EVA	ss5820424915	Oct 12, 2022 (156)
43	EVA	ss5852619542	Oct 12, 2022 (156)
44	EVA	ss5931355772	Oct 12, 2022 (156)
45	1000Genomes	NC_000002.11 - 86838134	Oct 11, 2018 (152)
46	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 5123577 (NC_000002.11:86838133::A 1482/3854) Row 5123578 (NC_000002.11:86838133::AA 182/3854)	-	Oct 11, 2018 (152)
47	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 5123577 (NC_000002.11:86838133::A 1482/3854) Row 5123578 (NC_000002.11:86838133::AA 182/3854)	-	Oct 11, 2018 (152)
48	The Danish reference pan genome	NC_000002.11 - 86838134	Apr 25, 2020 (154)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65351521 (NC_000002.12:86611010::A 64917/118648) Row 65351522 (NC_000002.12:86611010::AA 367/118834) Row 65351523 (NC_000002.12:86611010::AAA 20/118860)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65351521 (NC_000002.12:86611010::A 64917/118648) Row 65351522 (NC_000002.12:86611010::AA 367/118834) Row 65351523 (NC_000002.12:86611010::AAA 20/118860)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65351521 (NC_000002.12:86611010::A 64917/118648) Row 65351522 (NC_000002.12:86611010::AA 367/118834) Row 65351523 (NC_000002.12:86611010::AAA 20/118860)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65351521 (NC_000002.12:86611010::A 64917/118648) Row 65351522 (NC_000002.12:86611010::AA 367/118834) Row 65351523 (NC_000002.12:86611010::AAA 20/118860)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65351521 (NC_000002.12:86611010::A 64917/118648) Row 65351522 (NC_000002.12:86611010::AA 367/118834) Row 65351523 (NC_000002.12:86611010::AAA 20/118860)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 65351521 (NC_000002.12:86611010::A 64917/118648) Row 65351522 (NC_000002.12:86611010::AA 367/118834) Row 65351523 (NC_000002.12:86611010::AAA 20/118860)...	-	Apr 26, 2021 (155)
55	Northern Sweden	NC_000002.11 - 86838134	Jul 13, 2019 (153)
56	8.3KJPN Submission ignored due to conflicting rows: Row 10443606 (NC_000002.11:86838133::A 11751/16732) Row 10443607 (NC_000002.11:86838133:A: 3/16732) Row 10443608 (NC_000002.11:86838133::AA 86/16732)	-	Apr 26, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 10443606 (NC_000002.11:86838133::A 11751/16732) Row 10443607 (NC_000002.11:86838133:A: 3/16732) Row 10443608 (NC_000002.11:86838133::AA 86/16732)	-	Apr 26, 2021 (155)
58	8.3KJPN Submission ignored due to conflicting rows: Row 10443606 (NC_000002.11:86838133::A 11751/16732) Row 10443607 (NC_000002.11:86838133:A: 3/16732) Row 10443608 (NC_000002.11:86838133::AA 86/16732)	-	Apr 26, 2021 (155)
59	14KJPN Submission ignored due to conflicting rows: Row 15251688 (NC_000002.12:86611010::A 19434/28160) Row 15251689 (NC_000002.12:86611010:A: 4/28160) Row 15251690 (NC_000002.12:86611010::AA 130/28160)	-	Oct 12, 2022 (156)
60	14KJPN Submission ignored due to conflicting rows: Row 15251688 (NC_000002.12:86611010::A 19434/28160) Row 15251689 (NC_000002.12:86611010:A: 4/28160) Row 15251690 (NC_000002.12:86611010::AA 130/28160)	-	Oct 12, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 15251688 (NC_000002.12:86611010::A 19434/28160) Row 15251689 (NC_000002.12:86611010:A: 4/28160) Row 15251690 (NC_000002.12:86611010::AA 130/28160)	-	Oct 12, 2022 (156)
62	UK 10K study - Twins Submission ignored due to conflicting rows: Row 5123577 (NC_000002.11:86838133::A 1430/3708) Row 5123578 (NC_000002.11:86838133::AA 194/3708)	-	Oct 11, 2018 (152)
63	UK 10K study - Twins Submission ignored due to conflicting rows: Row 5123577 (NC_000002.11:86838133::A 1430/3708) Row 5123578 (NC_000002.11:86838133::AA 194/3708)	-	Oct 11, 2018 (152)
64	ALFA	NC_000002.12 - 86611011	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)
rs66892874	May 11, 2012 (137)
rs66892875	Feb 26, 2009 (130)
rs72363376	May 11, 2012 (137)
rs139497526	Sep 17, 2011 (135)
rs149698385	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4045629274	NC_000002.12:86611010:AAA:	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
11943246588	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4045629273	NC_000002.12:86611010:AA:	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
11943246588	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss5152474300	NC_000002.11:86838133:A:	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3704371150, ss4045629272, ss5248918654, ss5449037868, ss5681414585	NC_000002.12:86611010:A:	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
11943246588	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss294993143	NC_000002.10:86691645::A	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss288190135, ss294993144	NC_000002.10:86691660::A	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
9211304, 681244, 1926715, ss663333264, ss1368460562, ss1575453627, ss1702842051, ss1702842061, ss2030427509, ss2989897578, ss3728641850, ss3827101229, ss5152474299, ss5820424914	NC_000002.11:86838133::A	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3647081760, ss3801429414, ss4045629269, ss5248918653, ss5449037867, ss5681414584, ss5852619542, ss5931355772	NC_000002.12:86611010::A	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
11943246588	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3704371149	NC_000002.12:86611011::A	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss41683565, ss95278769	NT_022184.15:65660036::A	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss1702842055, ss1702842065, ss2989897579, ss5152474301, ss5820424915	NC_000002.11:86838133::AA	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4045629270, ss5248918655, ss5449037869, ss5681414586	NC_000002.12:86611010::AA	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
11943246588	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3704371148	NC_000002.12:86611011::AA	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4045629271	NC_000002.12:86611010::AAA	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
11943246588	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000002.12:86611010:AAAAAAAAAAAA… NC_000002.12:86611010:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(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 rs36001734

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

rs36001734