Name: rs536176
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.

rs536176

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:109113798 (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: T>A / T>C / T>G
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.485938 (128623/264690, TOPMED)
C=0.48404 (13676/28254, 14KJPN)
C=0.35427 (8997/25396, ALFA) (+ 15 more)
C=0.48747 (8169/16758, 8.3KJPN)
T=0.4617 (2957/6404, 1000G_30x)
T=0.4629 (2318/5008, 1000G)
C=0.3592 (1609/4480, Estonian)
C=0.3376 (1301/3854, ALSPAC)
C=0.3581 (1328/3708, TWINSUK)
C=0.4409 (1290/2926, KOREAN)
C=0.4415 (808/1830, Korea1K)
C=0.313 (188/600, NorthernSweden)
C=0.354 (189/534, MGP)
T=0.291 (117/402, SGDP_PRJ)
C=0.463 (100/216, Qatari)
C=0.481 (103/214, Vietnamese)
C=0.15 (6/40, GENOME_DK)
T=0.34 (13/38, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CFAP276 : Non Coding Transcript Variant
ELAPOR1 : 2KB Upstream 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: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	25396	T=0.64573	A=0.00000, C=0.35427, G=0.00000
European	Sub	20176	T=0.68928	A=0.00000, C=0.31072, G=0.00000
African	Sub	3286	T=0.3789	A=0.0000, C=0.6211, G=0.0000
African Others	Sub	110	T=0.291	A=0.000, C=0.709, G=0.000
African American	Sub	3176	T=0.3819	A=0.0000, C=0.6181, G=0.0000
Asian	Sub	38	T=0.68	A=0.00, C=0.32, G=0.00
East Asian	Sub	26	T=0.62	A=0.00, C=0.38, G=0.00
Other Asian	Sub	12	T=0.83	A=0.00, C=0.17, G=0.00
Latin American 1	Sub	48	T=0.75	A=0.00, C=0.25, G=0.00
Latin American 2	Sub	244	T=0.832	A=0.000, C=0.168, G=0.000
South Asian	Sub	44	T=0.68	A=0.00, C=0.32, G=0.00
Other	Sub	1560	T=0.6103	A=0.0000, C=0.3897, G=0.0000

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
TopMed	Global	Study-wide	264690	T=0.514062	C=0.485938
14KJPN	JAPANESE	Study-wide	28254	T=0.51596	C=0.48404
Allele Frequency Aggregator	Total	Global	25396	T=0.64573	A=0.00000, C=0.35427, G=0.00000
Allele Frequency Aggregator	European	Sub	20176	T=0.68928	A=0.00000, C=0.31072, G=0.00000
Allele Frequency Aggregator	African	Sub	3286	T=0.3789	A=0.0000, C=0.6211, G=0.0000
Allele Frequency Aggregator	Other	Sub	1560	T=0.6103	A=0.0000, C=0.3897, G=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	244	T=0.832	A=0.000, C=0.168, G=0.000
Allele Frequency Aggregator	Latin American 1	Sub	48	T=0.75	A=0.00, C=0.25, G=0.00
Allele Frequency Aggregator	South Asian	Sub	44	T=0.68	A=0.00, C=0.32, G=0.00
Allele Frequency Aggregator	Asian	Sub	38	T=0.68	A=0.00, C=0.32, G=0.00
8.3KJPN	JAPANESE	Study-wide	16758	T=0.51253	C=0.48747
1000Genomes_30x	Global	Study-wide	6404	T=0.4617	C=0.5383
1000Genomes_30x	African	Sub	1786	T=0.2424	C=0.7576
1000Genomes_30x	Europe	Sub	1266	T=0.6311	C=0.3689
1000Genomes_30x	South Asian	Sub	1202	T=0.4983	C=0.5017
1000Genomes_30x	East Asian	Sub	1170	T=0.5171	C=0.4829
1000Genomes_30x	American	Sub	980	T=0.532	C=0.468
1000Genomes	Global	Study-wide	5008	T=0.4629	C=0.5371
1000Genomes	African	Sub	1322	T=0.2496	C=0.7504
1000Genomes	East Asian	Sub	1008	T=0.5179	C=0.4821
1000Genomes	Europe	Sub	1006	T=0.6282	C=0.3718
1000Genomes	South Asian	Sub	978	T=0.487	C=0.513
1000Genomes	American	Sub	694	T=0.516	C=0.484
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.6408	C=0.3592
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.6624	C=0.3376
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.6419	C=0.3581
KOREAN population from KRGDB	KOREAN	Study-wide	2926	T=0.5591	A=0.0000, C=0.4409
Korean Genome Project	KOREAN	Study-wide	1830	T=0.5585	C=0.4415
Northern Sweden	ACPOP	Study-wide	600	T=0.687	C=0.313
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	T=0.646	C=0.354
SGDP_PRJ	Global	Study-wide	402	T=0.291	C=0.709
Qatari	Global	Study-wide	216	T=0.537	C=0.463
A Vietnamese Genetic Variation Database	Global	Study-wide	214	T=0.519	C=0.481
The Danish reference pan genome	Danish	Study-wide	40	T=0.85	C=0.15
Siberian	Global	Study-wide	38	T=0.34	C=0.66

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.109113798T>A
GRCh38.p14 chr 1	NC_000001.11:g.109113798T>C
GRCh38.p14 chr 1	NC_000001.11:g.109113798T>G
GRCh37.p13 chr 1	NC_000001.10:g.109656420T>A
GRCh37.p13 chr 1	NC_000001.10:g.109656420T>C
GRCh37.p13 chr 1	NC_000001.10:g.109656420T>G
ELAPOR1 RefSeqGene	NG_032763.1:g.4836T>A
ELAPOR1 RefSeqGene	NG_032763.1:g.4836T>C
ELAPOR1 RefSeqGene	NG_032763.1:g.4836T>G

Gene: CFAP276, cilia and flagella associated protein 276 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CFAP276 transcript variant 2	NM_001366200.3:c.-121=	N/A	5 Prime UTR Variant
CFAP276 transcript variant 3	NM_001122961.3:c.-121=	N/A	5 Prime UTR Variant
CFAP276 transcript variant 5	NM_001366202.3:c.-121=	N/A	5 Prime UTR Variant
CFAP276 transcript variant 1	NM_001245025.3:c.	N/A	Genic Upstream Transcript Variant
CFAP276 transcript variant 4	NM_001366201.3:c.	N/A	Genic Upstream Transcript Variant
CFAP276 transcript variant 6	NR_158762.3:n.34A>T	N/A	Non Coding Transcript Variant
CFAP276 transcript variant 6	NR_158762.3:n.34A>G	N/A	Non Coding Transcript Variant
CFAP276 transcript variant 6	NR_158762.3:n.34A>C	N/A	Non Coding Transcript Variant
CFAP276 transcript variant 7	NR_158763.3:n.	N/A	Genic Upstream Transcript Variant
CFAP276 transcript variant X1	XM_011540647.3:c.	N/A	Genic Upstream Transcript Variant

Gene: ELAPOR1, endosome-lysosome associated apoptosis and autophagy regulator 1 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
ELAPOR1 transcript variant 2	NM_001267048.2:c.	N/A	Upstream Transcript Variant
ELAPOR1 transcript variant 4	NM_001284352.2:c.	N/A	Upstream Transcript Variant
ELAPOR1 transcript variant 1	NM_020775.5:c.	N/A	Upstream Transcript Variant
ELAPOR1 transcript variant 5	NM_001284353.2:c.	N/A	N/A
ELAPOR1 transcript variant X1	XM_011541825.3:c.	N/A	Upstream Transcript Variant
ELAPOR1 transcript variant X2	XM_011541826.4:c.	N/A	Upstream Transcript Variant
ELAPOR1 transcript variant X3	XM_011541827.3:c.	N/A	Upstream Transcript Variant
ELAPOR1 transcript variant X4	XM_047426133.1:c.	N/A	N/A

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=	A	C	G
GRCh38.p14 chr 1	NC_000001.11:g.109113798=	NC_000001.11:g.109113798T>A	NC_000001.11:g.109113798T>C	NC_000001.11:g.109113798T>G
GRCh37.p13 chr 1	NC_000001.10:g.109656420=	NC_000001.10:g.109656420T>A	NC_000001.10:g.109656420T>C	NC_000001.10:g.109656420T>G
ELAPOR1 RefSeqGene	NG_032763.1:g.4836=	NG_032763.1:g.4836T>A	NG_032763.1:g.4836T>C	NG_032763.1:g.4836T>G
CFAP276 transcript variant 2	NM_001366200.3:c.-121=	NM_001366200.3:c.-121A>T	NM_001366200.3:c.-121A>G	NM_001366200.3:c.-121A>C
C1orf194 transcript variant 2	NM_001366200.2:c.-121=	NM_001366200.2:c.-121A>T	NM_001366200.2:c.-121A>G	NM_001366200.2:c.-121A>C
C1orf194 transcript variant 2	NM_001366200.1:c.-121=	NM_001366200.1:c.-121A>T	NM_001366200.1:c.-121A>G	NM_001366200.1:c.-121A>C
CFAP276 transcript variant 3	NM_001122961.3:c.-121=	NM_001122961.3:c.-121A>T	NM_001122961.3:c.-121A>G	NM_001122961.3:c.-121A>C
C1orf194 transcript variant 3	NM_001122961.2:c.-121=	NM_001122961.2:c.-121A>T	NM_001122961.2:c.-121A>G	NM_001122961.2:c.-121A>C
C1orf194 transcript variant 3	NM_001122961.1:c.-121=	NM_001122961.1:c.-121A>T	NM_001122961.1:c.-121A>G	NM_001122961.1:c.-121A>C
CFAP276 transcript variant 5	NM_001366202.3:c.-121=	NM_001366202.3:c.-121A>T	NM_001366202.3:c.-121A>G	NM_001366202.3:c.-121A>C
C1orf194 transcript variant 5	NM_001366202.2:c.-121=	NM_001366202.2:c.-121A>T	NM_001366202.2:c.-121A>G	NM_001366202.2:c.-121A>C
C1orf194 transcript variant 5	NM_001366202.1:c.-121=	NM_001366202.1:c.-121A>T	NM_001366202.1:c.-121A>G	NM_001366202.1:c.-121A>C
CFAP276 transcript variant 6	NR_158762.3:n.34=	NR_158762.3:n.34A>T	NR_158762.3:n.34A>G	NR_158762.3:n.34A>C
C1orf194 transcript variant 6	NR_158762.2:n.34=	NR_158762.2:n.34A>T	NR_158762.2:n.34A>G	NR_158762.2:n.34A>C
C1orf194 transcript variant 6	NR_158762.1:n.34=	NR_158762.1:n.34A>T	NR_158762.1:n.34A>G	NR_158762.1:n.34A>C

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#.

85 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_JCM	ss706806	Aug 11, 2000 (83)
2	YUSUKE	ss3251130	Sep 28, 2001 (100)
3	BCM_SSAHASNP	ss9893851	Jul 11, 2003 (116)
4	HUMANGENOME_JCVI	ss99238922	Feb 06, 2009 (130)
5	GMI	ss155511869	Dec 01, 2009 (131)
6	COMPLETE_GENOMICS	ss164993936	Jul 04, 2010 (132)
7	COMPLETE_GENOMICS	ss166979772	Jul 04, 2010 (132)
8	BUSHMAN	ss198917238	Jul 04, 2010 (132)
9	1000GENOMES	ss230686060	Jul 14, 2010 (132)
10	GMI	ss275973051	May 04, 2012 (137)
11	PJP	ss290595455	May 09, 2011 (134)
12	ILLUMINA	ss410764753	Sep 17, 2011 (135)
13	ILLUMINA	ss482064512	May 04, 2012 (137)
14	ILLUMINA	ss484050205	May 04, 2012 (137)
15	ILLUMINA	ss536241470	Sep 08, 2015 (146)
16	SSMP	ss648303395	Apr 25, 2013 (138)
17	ILLUMINA	ss780664399	Sep 08, 2015 (146)
18	ILLUMINA	ss782469763	Aug 21, 2014 (142)
19	ILLUMINA	ss783603922	Sep 08, 2015 (146)
20	ILLUMINA	ss836160043	Sep 08, 2015 (146)
21	EVA-GONL	ss975555682	Aug 21, 2014 (142)
22	JMKIDD_LAB	ss1068182002	Aug 21, 2014 (142)
23	1000GENOMES	ss1292374158	Aug 21, 2014 (142)
24	DDI	ss1425932920	Apr 01, 2015 (144)
25	EVA_GENOME_DK	ss1574313817	Apr 01, 2015 (144)
26	EVA_DECODE	ss1584934838	Apr 01, 2015 (144)
27	EVA_UK10K_ALSPAC	ss1600958021	Apr 01, 2015 (144)
28	EVA_UK10K_TWINSUK	ss1643952054	Apr 01, 2015 (144)
29	EVA_MGP	ss1710914709	Apr 01, 2015 (144)
30	HAMMER_LAB	ss1794909171	Sep 08, 2015 (146)
31	WEILL_CORNELL_DGM	ss1918755669	Feb 12, 2016 (147)
32	GENOMED	ss1966838346	Jul 19, 2016 (147)
33	JJLAB	ss2019902266	Sep 14, 2016 (149)
34	USC_VALOUEV	ss2147919762	Dec 20, 2016 (150)
35	HUMAN_LONGEVITY	ss2165592209	Dec 20, 2016 (150)
36	SYSTEMSBIOZJU	ss2624460462	Nov 08, 2017 (151)
37	ILLUMINA	ss2632560892	Nov 08, 2017 (151)
38	GRF	ss2697849570	Nov 08, 2017 (151)
39	GNOMAD	ss2759394731	Nov 08, 2017 (151)
40	SWEGEN	ss2987414826	Nov 08, 2017 (151)
41	BIOINF_KMB_FNS_UNIBA	ss3023714933	Nov 08, 2017 (151)
42	CSHL	ss3343628590	Nov 08, 2017 (151)
43	ILLUMINA	ss3626178611	Oct 11, 2018 (152)
44	ILLUMINA	ss3630594753	Oct 11, 2018 (152)
45	OMUKHERJEE_ADBS	ss3646234332	Oct 11, 2018 (152)
46	URBANLAB	ss3646748953	Oct 11, 2018 (152)
47	EGCUT_WGS	ss3655503295	Jul 12, 2019 (153)
48	EVA_DECODE	ss3687501689	Jul 12, 2019 (153)
49	ACPOP	ss3727376628	Jul 12, 2019 (153)
50	EVA	ss3746654333	Jul 12, 2019 (153)
51	PACBIO	ss3783515280	Jul 12, 2019 (153)
52	PACBIO	ss3789157758	Jul 12, 2019 (153)
53	PACBIO	ss3794030664	Jul 12, 2019 (153)
54	KHV_HUMAN_GENOMES	ss3799658837	Jul 12, 2019 (153)
55	EVA	ss3825570900	Apr 25, 2020 (154)
56	EVA	ss3826361770	Apr 25, 2020 (154)
57	EVA	ss3836572340	Apr 25, 2020 (154)
58	EVA	ss3841980654	Apr 25, 2020 (154)
59	SGDP_PRJ	ss3849620584	Apr 25, 2020 (154)
60	KRGDB	ss3894709961	Apr 25, 2020 (154)
61	KOGIC	ss3945216769	Apr 25, 2020 (154)
62	FSA-LAB	ss3983939497	Apr 25, 2021 (155)
63	FSA-LAB	ss3983939498	Apr 25, 2021 (155)
64	EVA	ss3986011621	Apr 25, 2021 (155)
65	EVA	ss3986129994	Apr 25, 2021 (155)
66	TOPMED	ss4463092610	Apr 25, 2021 (155)
67	TOMMO_GENOMICS	ss5145616140	Apr 25, 2021 (155)
68	EVA	ss5237162946	Apr 25, 2021 (155)
69	1000G_HIGH_COVERAGE	ss5243560475	Oct 12, 2022 (156)
70	EVA	ss5314642460	Oct 12, 2022 (156)
71	EVA	ss5321093049	Oct 12, 2022 (156)
72	HUGCELL_USP	ss5444488685	Oct 12, 2022 (156)
73	1000G_HIGH_COVERAGE	ss5516528473	Oct 12, 2022 (156)
74	EVA	ss5623995269	Oct 12, 2022 (156)
75	SANFORD_IMAGENETICS	ss5626270852	Oct 12, 2022 (156)
76	TOMMO_GENOMICS	ss5670864717	Oct 12, 2022 (156)
77	EVA	ss5800083752	Oct 12, 2022 (156)
78	YY_MCH	ss5800919860	Oct 12, 2022 (156)
79	EVA	ss5832464166	Oct 12, 2022 (156)
80	EVA	ss5848267004	Oct 12, 2022 (156)
81	EVA	ss5849062035	Oct 12, 2022 (156)
82	EVA	ss5909741951	Oct 12, 2022 (156)
83	EVA	ss5938134834	Oct 12, 2022 (156)
84	EVA	ss5979977018	Oct 12, 2022 (156)
85	EVA	ss5981195543	Oct 12, 2022 (156)
86	1000Genomes	NC_000001.10 - 109656420	Oct 11, 2018 (152)
87	1000Genomes_30x	NC_000001.11 - 109113798	Oct 12, 2022 (156)
88	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 109656420	Oct 11, 2018 (152)
89	Genetic variation in the Estonian population	NC_000001.10 - 109656420	Oct 11, 2018 (152)
90	The Danish reference pan genome	NC_000001.10 - 109656420	Apr 25, 2020 (154)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22273315 (NC_000001.11:109113797:T:A 2/140082) Row 22273316 (NC_000001.11:109113797:T:C 66708/140038) Row 22273317 (NC_000001.11:109113797:T:G 1/140082)	-	Apr 25, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22273315 (NC_000001.11:109113797:T:A 2/140082) Row 22273316 (NC_000001.11:109113797:T:C 66708/140038) Row 22273317 (NC_000001.11:109113797:T:G 1/140082)	-	Apr 25, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 22273315 (NC_000001.11:109113797:T:A 2/140082) Row 22273316 (NC_000001.11:109113797:T:C 66708/140038) Row 22273317 (NC_000001.11:109113797:T:G 1/140082)	-	Apr 25, 2021 (155)
94	KOREAN population from KRGDB	NC_000001.10 - 109656420	Apr 25, 2020 (154)
95	Korean Genome Project	NC_000001.11 - 109113798	Apr 25, 2020 (154)
96	Medical Genome Project healthy controls from Spanish population	NC_000001.10 - 109656420	Apr 25, 2020 (154)
97	Northern Sweden	NC_000001.10 - 109656420	Jul 12, 2019 (153)
98	Qatari	NC_000001.10 - 109656420	Apr 25, 2020 (154)
99	SGDP_PRJ	NC_000001.10 - 109656420	Apr 25, 2020 (154)
100	Siberian	NC_000001.10 - 109656420	Apr 25, 2020 (154)
101	8.3KJPN	NC_000001.10 - 109656420	Apr 25, 2021 (155)
102	14KJPN	NC_000001.11 - 109113798	Oct 12, 2022 (156)
103	TopMed	NC_000001.11 - 109113798	Apr 25, 2021 (155)
104	UK 10K study - Twins	NC_000001.10 - 109656420	Oct 11, 2018 (152)
105	A Vietnamese Genetic Variation Database	NC_000001.10 - 109656420	Jul 12, 2019 (153)
106	ALFA	NC_000001.11 - 109113798	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)
rs11544390	Oct 07, 2004 (123)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
1887355, ss3894709961	NC_000001.10:109656419:T:A	NC_000001.11:109113797:T:A	(self)
1572961672	NC_000001.11:109113797:T:A	NC_000001.11:109113797:T:A	(self)
ss164993936, ss166979772, ss198917238, ss275973051, ss290595455, ss410764753, ss482064512, ss1584934838	NC_000001.9:109457942:T:C	NC_000001.11:109113797:T:C	(self)
3148099, 1738919, 1241543, 1658913, 1887355, 31461, 661493, 797599, 1637564, 436116, 3585447, 1738919, 377390, ss230686060, ss484050205, ss536241470, ss648303395, ss780664399, ss782469763, ss783603922, ss836160043, ss975555682, ss1068182002, ss1292374158, ss1425932920, ss1574313817, ss1600958021, ss1643952054, ss1710914709, ss1794909171, ss1918755669, ss1966838346, ss2019902266, ss2147919762, ss2624460462, ss2632560892, ss2697849570, ss2759394731, ss2987414826, ss3343628590, ss3626178611, ss3630594753, ss3646234332, ss3655503295, ss3727376628, ss3746654333, ss3783515280, ss3789157758, ss3794030664, ss3825570900, ss3826361770, ss3836572340, ss3849620584, ss3894709961, ss3983939497, ss3983939498, ss3986011621, ss3986129994, ss5145616140, ss5314642460, ss5321093049, ss5623995269, ss5626270852, ss5800083752, ss5832464166, ss5848267004, ss5938134834, ss5979977018, ss5981195543	NC_000001.10:109656419:T:C	NC_000001.11:109113797:T:C	(self)
4054408, 1594770, 4701821, 26698945, 1572961672, ss2165592209, ss3023714933, ss3646748953, ss3687501689, ss3799658837, ss3841980654, ss3945216769, ss4463092610, ss5237162946, ss5243560475, ss5444488685, ss5516528473, ss5670864717, ss5800919860, ss5849062035, ss5909741951	NC_000001.11:109113797:T:C	NC_000001.11:109113797:T:C	(self)
ss9893851	NT_019273.15:94233:T:C	NC_000001.11:109113797:T:C	(self)
ss706806, ss3251130, ss99238922, ss155511869	NT_032977.9:79628337:T:C	NC_000001.11:109113797:T:C	(self)
1572961672	NC_000001.11:109113797:T:G	NC_000001.11:109113797:T:G	(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 rs536176

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
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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

rs536176