Name: rs34303036
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.

rs34303036

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr8:56314206-56314216 (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: delAA / delA / dupA / dupAA / dupA…
delAA / delA / dupA / dupAA / dupAAA
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.3946 (1779/4508, ALFA)
(A)₁₁=0.1931 (431/2232, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SDR16C5 : 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	4508	AAAAAAAAAAA=0.0410	AAAAAAAAA=0.0000, AAAAAAAAAA=0.3946, AAAAAAAAAAAA=0.5322, AAAAAAAAAAAAA=0.0322, AAAAAAAAAAAAAA=0.0000	0.190281	0.347826	0.461893	3
European	Sub	4460	AAAAAAAAAAA=0.0323	AAAAAAAAA=0.0000, AAAAAAAAAA=0.3980, AAAAAAAAAAAA=0.5372, AAAAAAAAAAAAA=0.0325, AAAAAAAAAAAAAA=0.0000	0.190061	0.348361	0.461578	3
African	Sub	38	AAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00	0	0	0	N/A
African Others	Sub	0	AAAAAAAAAAA=0	AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0	0	0	0	N/A
African American	Sub	38	AAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00	0	0	0	N/A
Asian	Sub	2	AAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0	0	0	0	N/A
East Asian	Sub	2	AAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0	0	0	0	N/A
Other Asian	Sub	0	AAAAAAAAAAA=0	AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	0	AAAAAAAAAAA=0	AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 2	Sub	0	AAAAAAAAAAA=0	AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0	0	0	0	N/A
South Asian	Sub	0	AAAAAAAAAAA=0	AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0	0	0	0	N/A
Other	Sub	8	AAAAAAAAAAA=0.1	AAAAAAAAA=0.0, AAAAAAAAAA=0.5, AAAAAAAAAAAA=0.4, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0	0.333333	0.0	0.666667	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	4508	(A)₁₁=0.0410	delAA=0.0000, delA=0.3946, dupA=0.5322, dupAA=0.0322, dupAAA=0.0000
Allele Frequency Aggregator	European	Sub	4460	(A)₁₁=0.0323	delAA=0.0000, delA=0.3980, dupA=0.5372, dupAA=0.0325, dupAAA=0.0000
Allele Frequency Aggregator	African	Sub	38	(A)₁₁=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Other	Sub	8	(A)₁₁=0.1	delAA=0.0, delA=0.5, dupA=0.4, dupAA=0.0, dupAAA=0.0
Allele Frequency Aggregator	Asian	Sub	2	(A)₁₁=1.0	delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	(A)₁₁=0	delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0
Allele Frequency Aggregator	Latin American 2	Sub	0	(A)₁₁=0	delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0
Allele Frequency Aggregator	South Asian	Sub	0	(A)₁₁=0	delAA=0, delA=0, dupA=0, dupAA=0, dupAAA=0
1000Genomes	Global	Study-wide	2232	(A)₁₁=0.1931	delA=0.8069
1000Genomes	African	Sub	644	(A)₁₁=0.352	delA=0.648
1000Genomes	East Asian	Sub	498	(A)₁₁=0.124	delA=0.876
1000Genomes	South Asian	Sub	446	(A)₁₁=0.155	delA=0.845
1000Genomes	Europe	Sub	435	(A)₁₁=0.092	delA=0.908
1000Genomes	American	Sub	209	(A)₁₁=0.158	delA=0.842

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 8	NC_000008.11:g.56314215_56314216del
GRCh38.p14 chr 8	NC_000008.11:g.56314216del
GRCh38.p14 chr 8	NC_000008.11:g.56314216dup
GRCh38.p14 chr 8	NC_000008.11:g.56314215_56314216dup
GRCh38.p14 chr 8	NC_000008.11:g.56314214_56314216dup
GRCh37.p13 chr 8	NC_000008.10:g.57226774_57226775del
GRCh37.p13 chr 8	NC_000008.10:g.57226775del
GRCh37.p13 chr 8	NC_000008.10:g.57226775dup
GRCh37.p13 chr 8	NC_000008.10:g.57226774_57226775dup
GRCh37.p13 chr 8	NC_000008.10:g.57226773_57226775dup

Gene: SDR16C5, short chain dehydrogenase/reductase family 16C member 5 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SDR16C5 transcript variant 1	NM_001318049.2:c.333+1808… NM_001318049.2:c.333+1808_333+1809del	N/A	Intron Variant
SDR16C5 transcript variant 3	NM_001318050.2:c.333+1808… NM_001318050.2:c.333+1808_333+1809del	N/A	Intron Variant
SDR16C5 transcript variant 2	NM_138969.4:c.333+1808_33… NM_138969.4:c.333+1808_333+1809del	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)₁₁=	delAA	delA	dupA	dupAA	dupAAA
GRCh38.p14 chr 8	NC_000008.11:g.56314206_56314216=	NC_000008.11:g.56314215_56314216del	NC_000008.11:g.56314216del	NC_000008.11:g.56314216dup	NC_000008.11:g.56314215_56314216dup	NC_000008.11:g.56314214_56314216dup
GRCh37.p13 chr 8	NC_000008.10:g.57226765_57226775=	NC_000008.10:g.57226774_57226775del	NC_000008.10:g.57226775del	NC_000008.10:g.57226775dup	NC_000008.10:g.57226774_57226775dup	NC_000008.10:g.57226773_57226775dup
SDR16C5 transcript variant 1	NM_001318049.2:c.333+1809=	NM_001318049.2:c.333+1808_333+1809del	NM_001318049.2:c.333+1809del	NM_001318049.2:c.333+1809dup	NM_001318049.2:c.333+1808_333+1809dup	NM_001318049.2:c.333+1807_333+1809dup
SDR16C5 transcript variant 3	NM_001318050.2:c.333+1809=	NM_001318050.2:c.333+1808_333+1809del	NM_001318050.2:c.333+1809del	NM_001318050.2:c.333+1809dup	NM_001318050.2:c.333+1808_333+1809dup	NM_001318050.2:c.333+1807_333+1809dup
SDR16C5 transcript	NM_138969.2:c.333+1809=	NM_138969.2:c.333+1808_333+1809del	NM_138969.2:c.333+1809del	NM_138969.2:c.333+1809dup	NM_138969.2:c.333+1808_333+1809dup	NM_138969.2:c.333+1807_333+1809dup
SDR16C5 transcript variant 2	NM_138969.4:c.333+1809=	NM_138969.4:c.333+1808_333+1809del	NM_138969.4:c.333+1809del	NM_138969.4:c.333+1809dup	NM_138969.4:c.333+1808_333+1809dup	NM_138969.4:c.333+1807_333+1809dup
SDR16C5 transcript variant X1	XM_005251180.1:c.333+1809=	XM_005251180.1:c.333+1808_333+1809del	XM_005251180.1:c.333+1809del	XM_005251180.1:c.333+1809dup	XM_005251180.1:c.333+1808_333+1809dup	XM_005251180.1:c.333+1807_333+1809dup
SDR16C5 transcript variant X2	XM_005251181.1:c.333+1809=	XM_005251181.1:c.333+1808_333+1809del	XM_005251181.1:c.333+1809del	XM_005251181.1:c.333+1809dup	XM_005251181.1:c.333+1808_333+1809dup	XM_005251181.1:c.333+1807_333+1809dup

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#.

60 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss43240637	Dec 04, 2013 (138)
2	ABI	ss43307069	Mar 14, 2006 (126)
3	DEVINE_LAB	ss50187511	Mar 15, 2016 (147)
4	HGSV	ss81714301	Dec 04, 2013 (138)
5	HUMANGENOME_JCVI	ss95492832	Dec 05, 2013 (138)
6	BL	ss256068192	May 09, 2011 (137)
7	GMI	ss288908672	May 04, 2012 (137)
8	GMI	ss288908673	May 04, 2012 (137)
9	PJP	ss295382076	May 09, 2011 (134)
10	PJP	ss295382077	May 09, 2011 (137)
11	PJP	ss295382078	May 09, 2011 (137)
12	PJP	ss295382079	May 09, 2011 (137)
13	BILGI_BIOE	ss666438255	Apr 25, 2013 (138)
14	1000GENOMES	ss1367942017	Aug 21, 2014 (142)
15	1000GENOMES	ss1367942018	Aug 21, 2014 (142)
16	DDI	ss1536586214	Apr 01, 2015 (144)
17	EVA_UK10K_ALSPAC	ss1706061827	Apr 01, 2015 (144)
18	EVA_UK10K_TWINSUK	ss1706062191	Apr 01, 2015 (144)
19	EVA_UK10K_TWINSUK	ss1710382026	Apr 01, 2015 (144)
20	EVA_UK10K_TWINSUK	ss1710382027	Apr 01, 2015 (144)
21	EVA_UK10K_ALSPAC	ss1710382128	Apr 01, 2015 (144)
22	EVA_UK10K_ALSPAC	ss1710382130	Apr 01, 2015 (144)
23	HAMMER_LAB	ss1805543618	Sep 08, 2015 (146)
24	HAMMER_LAB	ss1805543619	Sep 08, 2015 (146)
25	SWEGEN	ss3003219589	Nov 08, 2017 (151)
26	BIOINF_KMB_FNS_UNIBA	ss3646096134	Oct 12, 2018 (152)
27	BIOINF_KMB_FNS_UNIBA	ss3646096135	Oct 12, 2018 (152)
28	EVA_DECODE	ss3722062322	Jul 13, 2019 (153)
29	EVA_DECODE	ss3722062323	Jul 13, 2019 (153)
30	EVA_DECODE	ss3722062324	Jul 13, 2019 (153)
31	PACBIO	ss3786152232	Jul 13, 2019 (153)
32	PACBIO	ss3791407205	Jul 13, 2019 (153)
33	PACBIO	ss3791407206	Jul 13, 2019 (153)
34	PACBIO	ss3796288544	Jul 13, 2019 (153)
35	PACBIO	ss3796288545	Jul 13, 2019 (153)
36	KHV_HUMAN_GENOMES	ss3811185851	Jul 13, 2019 (153)
37	KHV_HUMAN_GENOMES	ss3811185852	Jul 13, 2019 (153)
38	EVA	ss3831175073	Apr 26, 2020 (154)
39	KOGIC	ss3963923083	Apr 26, 2020 (154)
40	KOGIC	ss3963923084	Apr 26, 2020 (154)
41	KOGIC	ss3963923085	Apr 26, 2020 (154)
42	GNOMAD	ss4184806146	Apr 26, 2021 (155)
43	GNOMAD	ss4184806147	Apr 26, 2021 (155)
44	GNOMAD	ss4184806148	Apr 26, 2021 (155)
45	GNOMAD	ss4184806149	Apr 26, 2021 (155)
46	GNOMAD	ss4184806150	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5188817856	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5188817857	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5188817858	Apr 26, 2021 (155)
50	1000G_HIGH_COVERAGE	ss5277224876	Oct 14, 2022 (156)
51	1000G_HIGH_COVERAGE	ss5277224877	Oct 14, 2022 (156)
52	HUGCELL_USP	ss5473783468	Oct 14, 2022 (156)
53	HUGCELL_USP	ss5473783469	Oct 14, 2022 (156)
54	HUGCELL_USP	ss5473783470	Oct 14, 2022 (156)
55	TOMMO_GENOMICS	ss5730914444	Oct 14, 2022 (156)
56	TOMMO_GENOMICS	ss5730914445	Oct 14, 2022 (156)
57	TOMMO_GENOMICS	ss5730914446	Oct 14, 2022 (156)
58	EVA	ss5830565465	Oct 14, 2022 (156)
59	EVA	ss5830565466	Oct 14, 2022 (156)
60	EVA	ss5830565467	Oct 14, 2022 (156)
61	1000Genomes	NC_000008.10 - 57226765	Oct 12, 2018 (152)
62	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 23399221 (NC_000008.10:57226764:A: 1482/3854) Row 23399222 (NC_000008.10:57226764::A 2116/3854) Row 23399223 (NC_000008.10:57226764::AA 155/3854)	-	Oct 12, 2018 (152)
63	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 23399221 (NC_000008.10:57226764:A: 1482/3854) Row 23399222 (NC_000008.10:57226764::A 2116/3854) Row 23399223 (NC_000008.10:57226764::AA 155/3854)	-	Oct 12, 2018 (152)
64	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 23399221 (NC_000008.10:57226764:A: 1482/3854) Row 23399222 (NC_000008.10:57226764::A 2116/3854) Row 23399223 (NC_000008.10:57226764::AA 155/3854)	-	Oct 12, 2018 (152)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 296714315 (NC_000008.11:56314205::A 76812/138354) Row 296714316 (NC_000008.11:56314205::AA 3308/138444) Row 296714317 (NC_000008.11:56314205::AAA 2/138506)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 296714315 (NC_000008.11:56314205::A 76812/138354) Row 296714316 (NC_000008.11:56314205::AA 3308/138444) Row 296714317 (NC_000008.11:56314205::AAA 2/138506)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 296714315 (NC_000008.11:56314205::A 76812/138354) Row 296714316 (NC_000008.11:56314205::AA 3308/138444) Row 296714317 (NC_000008.11:56314205::AAA 2/138506)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 296714315 (NC_000008.11:56314205::A 76812/138354) Row 296714316 (NC_000008.11:56314205::AA 3308/138444) Row 296714317 (NC_000008.11:56314205::AAA 2/138506)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 296714315 (NC_000008.11:56314205::A 76812/138354) Row 296714316 (NC_000008.11:56314205::AA 3308/138444) Row 296714317 (NC_000008.11:56314205::AAA 2/138506)...	-	Apr 26, 2021 (155)
70	Korean Genome Project Submission ignored due to conflicting rows: Row 20301084 (NC_000008.11:56314206::A 955/1832) Row 20301085 (NC_000008.11:56314205:A: 774/1832) Row 20301086 (NC_000008.11:56314206::AA 22/1832)	-	Apr 26, 2020 (154)
71	Korean Genome Project Submission ignored due to conflicting rows: Row 20301084 (NC_000008.11:56314206::A 955/1832) Row 20301085 (NC_000008.11:56314205:A: 774/1832) Row 20301086 (NC_000008.11:56314206::AA 22/1832)	-	Apr 26, 2020 (154)
72	Korean Genome Project Submission ignored due to conflicting rows: Row 20301084 (NC_000008.11:56314206::A 955/1832) Row 20301085 (NC_000008.11:56314205:A: 774/1832) Row 20301086 (NC_000008.11:56314206::AA 22/1832)	-	Apr 26, 2020 (154)
73	8.3KJPN Submission ignored due to conflicting rows: Row 46787163 (NC_000008.10:57226764:A: 7104/16760) Row 46787164 (NC_000008.10:57226764::A 9072/16760) Row 46787165 (NC_000008.10:57226764::AA 77/16760)	-	Apr 26, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 46787163 (NC_000008.10:57226764:A: 7104/16760) Row 46787164 (NC_000008.10:57226764::A 9072/16760) Row 46787165 (NC_000008.10:57226764::AA 77/16760)	-	Apr 26, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 46787163 (NC_000008.10:57226764:A: 7104/16760) Row 46787164 (NC_000008.10:57226764::A 9072/16760) Row 46787165 (NC_000008.10:57226764::AA 77/16760)	-	Apr 26, 2021 (155)
76	14KJPN Submission ignored due to conflicting rows: Row 64751548 (NC_000008.11:56314205::A 15133/28258) Row 64751549 (NC_000008.11:56314205:A: 12163/28258) Row 64751550 (NC_000008.11:56314205::AA 119/28258)	-	Oct 14, 2022 (156)
77	14KJPN Submission ignored due to conflicting rows: Row 64751548 (NC_000008.11:56314205::A 15133/28258) Row 64751549 (NC_000008.11:56314205:A: 12163/28258) Row 64751550 (NC_000008.11:56314205::AA 119/28258)	-	Oct 14, 2022 (156)
78	14KJPN Submission ignored due to conflicting rows: Row 64751548 (NC_000008.11:56314205::A 15133/28258) Row 64751549 (NC_000008.11:56314205:A: 12163/28258) Row 64751550 (NC_000008.11:56314205::AA 119/28258)	-	Oct 14, 2022 (156)
79	UK 10K study - Twins Submission ignored due to conflicting rows: Row 23399221 (NC_000008.10:57226764:A: 1498/3708) Row 23399222 (NC_000008.10:57226764::A 1979/3708) Row 23399223 (NC_000008.10:57226764::AA 141/3708)	-	Oct 12, 2018 (152)
80	UK 10K study - Twins Submission ignored due to conflicting rows: Row 23399221 (NC_000008.10:57226764:A: 1498/3708) Row 23399222 (NC_000008.10:57226764::A 1979/3708) Row 23399223 (NC_000008.10:57226764::AA 141/3708)	-	Oct 12, 2018 (152)
81	UK 10K study - Twins Submission ignored due to conflicting rows: Row 23399221 (NC_000008.10:57226764:A: 1498/3708) Row 23399222 (NC_000008.10:57226764::A 1979/3708) Row 23399223 (NC_000008.10:57226764::AA 141/3708)	-	Oct 12, 2018 (152)
82	ALFA	NC_000008.11 - 56314206	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)
rs71258506	May 11, 2012 (137)
rs141289176	May 04, 2012 (137)
rs34499918	May 11, 2012 (137)
rs35675972	May 23, 2006 (127)
rs58776792	May 11, 2012 (137)
rs144057127	May 11, 2012 (137)
rs146444336	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4184806150	NC_000008.11:56314205:AA:	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAA	(self)
3602330615	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAA	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAA	(self)
ss256068192, ss288908672, ss295382076	NC_000008.9:57389318:A:	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAA	(self)
ss295382079	NC_000008.9:57389328:A:	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAA	(self)
42076494, ss666438255, ss1367942017, ss1536586214, ss1706061827, ss1706062191, ss1805543619, ss3003219589, ss3786152232, ss3791407205, ss3796288544, ss5188817856, ss5830565466	NC_000008.10:57226764:A:	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAA	(self)
ss3646096134, ss3722062324, ss3811185851, ss3963923084, ss4184806149, ss5473783468, ss5730914445	NC_000008.11:56314205:A:	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAA	(self)
3602330615	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAA	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAA	(self)
ss43307069	NT_008183.19:9091165:A:	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAA	(self)
ss95492832	NT_008183.19:9091175:A:	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAA	(self)
ss295382077	NC_000008.9:57389323::A	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss295382078	NC_000008.9:57389325::A	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss288908673	NC_000008.9:57389329::A	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss1805543618, ss3791407206, ss3796288545, ss3831175073, ss5188817857, ss5830565465	NC_000008.10:57226764::A	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss1367942018, ss1710382026, ss1710382128	NC_000008.10:57226765::A	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3646096135, ss4184806146, ss5277224876, ss5473783469, ss5730914444	NC_000008.11:56314205::A	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
3602330615	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAAAA	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3722062323, ss3811185852, ss3963923083	NC_000008.11:56314206::A	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss43240637, ss50187511	NT_008183.19:9091166::A	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss81714301	NT_008183.19:9091176::A	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss5188817858, ss5830565467	NC_000008.10:57226764::AA	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss1710382027, ss1710382130	NC_000008.10:57226765::AA	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4184806147, ss5277224877, ss5473783470, ss5730914446	NC_000008.11:56314205::AA	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAAAAA	(self)
3602330615	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAAAAA	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3722062322, ss3963923085	NC_000008.11:56314206::AA	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4184806148	NC_000008.11:56314205::AAA	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
3602330615	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000008.11:56314205:AAAAAAAAAAA:… NC_000008.11:56314205:AAAAAAAAAAA:AAAAAAAAAAAAAA	(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 rs34303036

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

rs34303036