Name: rs903603
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.

rs903603

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr9:27529318 (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: G>A / G>C
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.383449 (101495/264690, TOPMED)
A=0.475994 (97574/204990, ALFA)
A=0.388066 (54361/140082, GnomAD) (+ 17 more)
G=0.31340 (8856/28258, 14KJPN)
G=0.31569 (5291/16760, 8.3KJPN)
A=0.3935 (2520/6404, 1000G_30x)
A=0.4063 (2035/5008, 1000G)
G=0.4625 (2072/4480, Estonian)
G=0.3222 (944/2930, KOREAN)
A=0.4592 (957/2084, HGDP_Stanford)
A=0.3534 (668/1890, HapMap)
G=0.3224 (590/1830, Korea1K)
A=0.4771 (541/1134, Daghestan)
G=0.487 (292/600, NorthernSweden)
G=0.341 (124/364, SGDP_PRJ)
A=0.366 (79/216, Qatari)
A=0.481 (103/214, Vietnamese)
G=0.26 (11/42, Siberian)
G=0.45 (18/40, GENOME_DK)
A=0.42 (10/24, Ancient Sardinia)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MOB3B : Intron Variant
LOC124902107 : Synonymous Variant
Publications: 4 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	204990	G=0.524006	A=0.475994
European	Sub	178788	G=0.511209	A=0.488791
African	Sub	6530	G=0.8654	A=0.1346
African Others	Sub	236	G=0.953	A=0.047
African American	Sub	6294	G=0.8621	A=0.1379
Asian	Sub	520	G=0.387	A=0.613
East Asian	Sub	440	G=0.352	A=0.648
Other Asian	Sub	80	G=0.57	A=0.42
Latin American 1	Sub	686	G=0.618	A=0.382
Latin American 2	Sub	5552	G=0.5137	A=0.4863
South Asian	Sub	5018	G=0.5349	A=0.4651
Other	Sub	7896	G=0.5327	A=0.4673

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	G=0.616551	A=0.383449
Allele Frequency Aggregator	Total	Global	204990	G=0.524006	A=0.475994
Allele Frequency Aggregator	European	Sub	178788	G=0.511209	A=0.488791
Allele Frequency Aggregator	Other	Sub	7896	G=0.5327	A=0.4673
Allele Frequency Aggregator	African	Sub	6530	G=0.8654	A=0.1346
Allele Frequency Aggregator	Latin American 2	Sub	5552	G=0.5137	A=0.4863
Allele Frequency Aggregator	South Asian	Sub	5018	G=0.5349	A=0.4651
Allele Frequency Aggregator	Latin American 1	Sub	686	G=0.618	A=0.382
Allele Frequency Aggregator	Asian	Sub	520	G=0.387	A=0.613
gnomAD - Genomes	Global	Study-wide	140082	G=0.611934	A=0.388066
gnomAD - Genomes	European	Sub	75826	G=0.50736	A=0.49264
gnomAD - Genomes	African	Sub	42006	G=0.86231	A=0.13769
gnomAD - Genomes	American	Sub	13654	G=0.52607	A=0.47393
gnomAD - Genomes	Ashkenazi Jewish	Sub	3324	G=0.3700	A=0.6300
gnomAD - Genomes	East Asian	Sub	3126	G=0.4274	A=0.5726
gnomAD - Genomes	Other	Sub	2146	G=0.5960	A=0.4040
14KJPN	JAPANESE	Study-wide	28258	G=0.31340	A=0.68660
8.3KJPN	JAPANESE	Study-wide	16760	G=0.31569	A=0.68431
1000Genomes_30x	Global	Study-wide	6404	G=0.6065	A=0.3935
1000Genomes_30x	African	Sub	1786	G=0.9138	A=0.0862
1000Genomes_30x	Europe	Sub	1266	G=0.4921	A=0.5079
1000Genomes_30x	South Asian	Sub	1202	G=0.5424	A=0.4576
1000Genomes_30x	East Asian	Sub	1170	G=0.3991	A=0.6009
1000Genomes_30x	American	Sub	980	G=0.520	A=0.480
1000Genomes	Global	Study-wide	5008	G=0.5937	A=0.4063
1000Genomes	African	Sub	1322	G=0.9092	A=0.0908
1000Genomes	East Asian	Sub	1008	G=0.3879	A=0.6121
1000Genomes	Europe	Sub	1006	G=0.4881	A=0.5119
1000Genomes	South Asian	Sub	978	G=0.545	A=0.455
1000Genomes	American	Sub	694	G=0.513	A=0.487
Genetic variation in the Estonian population	Estonian	Study-wide	4480	G=0.4625	A=0.5375
KOREAN population from KRGDB	KOREAN	Study-wide	2930	G=0.3222	A=0.6778, C=0.0000
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	G=0.5408	A=0.4592
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	G=0.372	A=0.628
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	G=0.461	A=0.539
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	G=0.563	A=0.437
HGDP-CEPH-db Supplement 1	Europe	Sub	320	G=0.509	A=0.491
HGDP-CEPH-db Supplement 1	Africa	Sub	242	G=0.917	A=0.083
HGDP-CEPH-db Supplement 1	America	Sub	216	G=0.528	A=0.472
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	G=0.90	A=0.10
HapMap	Global	Study-wide	1890	G=0.6466	A=0.3534
HapMap	American	Sub	770	G=0.544	A=0.456
HapMap	African	Sub	690	G=0.907	A=0.093
HapMap	Asian	Sub	254	G=0.358	A=0.642
HapMap	Europe	Sub	176	G=0.489	A=0.511
Korean Genome Project	KOREAN	Study-wide	1830	G=0.3224	A=0.6776
Genome-wide autozygosity in Daghestan	Global	Study-wide	1134	G=0.5229	A=0.4771
Genome-wide autozygosity in Daghestan	Daghestan	Sub	626	G=0.554	A=0.446
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	G=0.493	A=0.507
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	G=0.451	A=0.549
Genome-wide autozygosity in Daghestan	Europe	Sub	108	G=0.491	A=0.509
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	G=0.52	A=0.48
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	G=0.44	A=0.56
Northern Sweden	ACPOP	Study-wide	600	G=0.487	A=0.513
SGDP_PRJ	Global	Study-wide	364	G=0.341	A=0.659
Qatari	Global	Study-wide	216	G=0.634	A=0.366
A Vietnamese Genetic Variation Database	Global	Study-wide	214	G=0.519	A=0.481
Siberian	Global	Study-wide	42	G=0.26	A=0.74
The Danish reference pan genome	Danish	Study-wide	40	G=0.45	A=0.55
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	24	G=0.58	A=0.42

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 9	NC_000009.12:g.27529318G>A
GRCh38.p14 chr 9	NC_000009.12:g.27529318G>C
GRCh37.p13 chr 9	NC_000009.11:g.27529316G>A
GRCh37.p13 chr 9	NC_000009.11:g.27529316G>C

Gene: MOB3B, MOB kinase activator 3B (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MOB3B transcript	NM_024761.5:c.-199+237C>T	N/A	Intron Variant
MOB3B transcript variant X1	XM_047423891.1:c.	N/A	Genic Upstream Transcript Variant
MOB3B transcript variant X2	XM_047423892.1:c.	N/A	Genic Upstream Transcript Variant
MOB3B transcript variant X3	XM_047423893.1:c.	N/A	Genic Upstream Transcript Variant
MOB3B transcript variant X4	XM_047423894.1:c.	N/A	Genic Upstream Transcript Variant
MOB3B transcript variant X5	XM_047423895.1:c.	N/A	Genic Upstream Transcript Variant

Gene: LOC124902107, uncharacterized LOC124902107 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC124902107 transcript	XM_047424279.1:c.570G>A	L [CTG] > L [CTA]	Coding Sequence Variant
dapper homolog 3-like	XP_047280235.1:p.Leu190=	L (Leu) > L (Leu)	Synonymous Variant
LOC124902107 transcript	XM_047424279.1:c.570G>C	L [CTG] > L [CTC]	Coding Sequence Variant
dapper homolog 3-like	XP_047280235.1:p.Leu190=	L (Leu) > L (Leu)	Synonymous 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	G=	A	C
GRCh38.p14 chr 9	NC_000009.12:g.27529318=	NC_000009.12:g.27529318G>A	NC_000009.12:g.27529318G>C
GRCh37.p13 chr 9	NC_000009.11:g.27529316=	NC_000009.11:g.27529316G>A	NC_000009.11:g.27529316G>C
LOC124902107 transcript	XM_047424279.1:c.570=	XM_047424279.1:c.570G>A	XM_047424279.1:c.570G>C
dapper homolog 3-like	XP_047280235.1:p.Leu190=	XP_047280235.1:p.Leu190=	XP_047280235.1:p.Leu190=
MOB3B transcript	NM_024761.4:c.-199+237=	NM_024761.4:c.-199+237C>T	NM_024761.4:c.-199+237C>G
MOB3B transcript	NM_024761.5:c.-199+237=	NM_024761.5:c.-199+237C>T	NM_024761.5:c.-199+237C>G
MOB3B transcript variant X1	XM_005251580.1:c.572+237=	XM_005251580.1:c.572+237C>T	XM_005251580.1:c.572+237C>G

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#.

109 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss1335982	Oct 05, 2000 (86)
2	SC_SNP	ss15540688	Feb 27, 2004 (120)
3	ABI	ss43888341	Mar 15, 2006 (126)
4	ILLUMINA	ss66661947	Nov 29, 2006 (127)
5	ILLUMINA	ss67891480	Nov 29, 2006 (127)
6	ILLUMINA	ss68027847	Nov 29, 2006 (127)
7	ILLUMINA	ss71592494	May 16, 2007 (127)
8	ILLUMINA	ss75501792	Dec 06, 2007 (129)
9	ILLUMINA	ss79288153	Dec 16, 2007 (130)
10	KRIBB_YJKIM	ss83603401	Dec 16, 2007 (130)
11	BCMHGSC_JDW	ss94035624	Mar 25, 2008 (129)
12	ILLUMINA	ss98232931	May 26, 2008 (130)
13	BGI	ss105672608	Feb 06, 2009 (130)
14	ILLUMINA	ss122942749	Dec 01, 2009 (131)
15	ENSEMBL	ss144040499	Dec 01, 2009 (131)
16	ILLUMINA	ss154479678	Dec 01, 2009 (131)
17	GMI	ss157352323	Dec 01, 2009 (131)
18	ILLUMINA	ss159654093	Dec 01, 2009 (131)
19	ILLUMINA	ss160965517	Dec 01, 2009 (131)
20	ILLUMINA	ss172426882	Jul 04, 2010 (132)
21	ILLUMINA	ss174776052	Jul 04, 2010 (132)
22	BUSHMAN	ss200275655	Jul 04, 2010 (132)
23	BCM-HGSC-SUB	ss206774860	Jul 04, 2010 (132)
24	1000GENOMES	ss224199318	Jul 14, 2010 (132)
25	1000GENOMES	ss234781110	Jul 15, 2010 (132)
26	1000GENOMES	ss241563020	Jul 15, 2010 (132)
27	BL	ss254144717	May 09, 2011 (134)
28	GMI	ss280166802	May 04, 2012 (137)
29	PJP	ss294425406	May 09, 2011 (134)
30	ILLUMINA	ss481834580	May 04, 2012 (137)
31	ILLUMINA	ss481867140	May 04, 2012 (137)
32	ILLUMINA	ss482825310	Sep 08, 2015 (146)
33	ILLUMINA	ss485711796	May 04, 2012 (137)
34	TISHKOFF	ss561331507	Apr 25, 2013 (138)
35	SSMP	ss655767532	Apr 25, 2013 (138)
36	ILLUMINA	ss783301517	Aug 21, 2014 (142)
37	ILLUMINA	ss825618671	Apr 01, 2015 (144)
38	ILLUMINA	ss832562869	Apr 01, 2015 (144)
39	ILLUMINA	ss833164895	Aug 21, 2014 (142)
40	ILLUMINA	ss833755723	Aug 21, 2014 (142)
41	EVA-GONL	ss986462601	Aug 21, 2014 (142)
42	JMKIDD_LAB	ss1076231331	Aug 21, 2014 (142)
43	1000GENOMES	ss1333485243	Aug 21, 2014 (142)
44	HAMMER_LAB	ss1397553329	Sep 08, 2015 (146)
45	DDI	ss1431795249	Apr 01, 2015 (144)
46	EVA_GENOME_DK	ss1583047245	Apr 01, 2015 (144)
47	EVA_SVP	ss1713102269	Apr 01, 2015 (144)
48	ILLUMINA	ss1752773718	Sep 08, 2015 (146)
49	HAMMER_LAB	ss1805944091	Sep 08, 2015 (146)
50	WEILL_CORNELL_DGM	ss1929746472	Feb 12, 2016 (147)
51	GENOMED	ss1971188899	Jul 19, 2016 (147)
52	JJLAB	ss2025584719	Sep 14, 2016 (149)
53	USC_VALOUEV	ss2153810312	Dec 20, 2016 (150)
54	HUMAN_LONGEVITY	ss2310599324	Dec 20, 2016 (150)
55	SYSTEMSBIOZJU	ss2627265497	Nov 08, 2017 (151)
56	ILLUMINA	ss2634855633	Nov 08, 2017 (151)
57	GRF	ss2709616667	Nov 08, 2017 (151)
58	GNOMAD	ss2877056802	Nov 08, 2017 (151)
59	SWEGEN	ss3004608902	Nov 08, 2017 (151)
60	BIOINF_KMB_FNS_UNIBA	ss3026581019	Nov 08, 2017 (151)
61	CSHL	ss3348589752	Nov 08, 2017 (151)
62	ILLUMINA	ss3625981577	Oct 12, 2018 (152)
63	ILLUMINA	ss3633530748	Oct 12, 2018 (152)
64	ILLUMINA	ss3634258869	Oct 12, 2018 (152)
65	ILLUMINA	ss3635209459	Oct 12, 2018 (152)
66	ILLUMINA	ss3635936964	Oct 12, 2018 (152)
67	ILLUMINA	ss3636955927	Oct 12, 2018 (152)
68	ILLUMINA	ss3637690254	Oct 12, 2018 (152)
69	ILLUMINA	ss3638808222	Oct 12, 2018 (152)
70	ILLUMINA	ss3639408989	Oct 12, 2018 (152)
71	ILLUMINA	ss3639736846	Oct 12, 2018 (152)
72	ILLUMINA	ss3640916749	Oct 12, 2018 (152)
73	ILLUMINA	ss3643735380	Oct 12, 2018 (152)
74	URBANLAB	ss3649102462	Oct 12, 2018 (152)
75	EGCUT_WGS	ss3672360288	Jul 13, 2019 (153)
76	ACPOP	ss3736431769	Jul 13, 2019 (153)
77	ILLUMINA	ss3744587562	Jul 13, 2019 (153)
78	ILLUMINA	ss3745509385	Jul 13, 2019 (153)
79	EVA	ss3769091219	Jul 13, 2019 (153)
80	ILLUMINA	ss3773001433	Jul 13, 2019 (153)
81	PACBIO	ss3786384469	Jul 13, 2019 (153)
82	PACBIO	ss3791605630	Jul 13, 2019 (153)
83	PACBIO	ss3796487307	Jul 13, 2019 (153)
84	KHV_HUMAN_GENOMES	ss3812249518	Jul 13, 2019 (153)
85	EVA	ss3831607933	Apr 26, 2020 (154)
86	EVA	ss3839321379	Apr 26, 2020 (154)
87	EVA	ss3844784205	Apr 26, 2020 (154)
88	HGDP	ss3847945512	Apr 26, 2020 (154)
89	SGDP_PRJ	ss3871825620	Apr 26, 2020 (154)
90	KRGDB	ss3919488435	Apr 26, 2020 (154)
91	KOGIC	ss3965560130	Apr 26, 2020 (154)
92	EVA	ss3985414631	Apr 26, 2021 (155)
93	EVA	ss4017433616	Apr 26, 2021 (155)
94	TOPMED	ss4817750793	Apr 26, 2021 (155)
95	TOMMO_GENOMICS	ss5192719017	Apr 26, 2021 (155)
96	1000G_HIGH_COVERAGE	ss5280292977	Oct 16, 2022 (156)
97	EVA	ss5315396193	Oct 16, 2022 (156)
98	EVA	ss5386952513	Oct 16, 2022 (156)
99	HUGCELL_USP	ss5476519988	Oct 16, 2022 (156)
100	EVA	ss5509677373	Oct 16, 2022 (156)
101	1000G_HIGH_COVERAGE	ss5572334123	Oct 16, 2022 (156)
102	SANFORD_IMAGENETICS	ss5647195166	Oct 16, 2022 (156)
103	TOMMO_GENOMICS	ss5735946501	Oct 16, 2022 (156)
104	EVA	ss5799781881	Oct 16, 2022 (156)
105	YY_MCH	ss5810465652	Oct 16, 2022 (156)
106	EVA	ss5829040948	Oct 16, 2022 (156)
107	EVA	ss5856729811	Oct 16, 2022 (156)
108	EVA	ss5916100649	Oct 16, 2022 (156)
109	EVA	ss5976476499	Oct 16, 2022 (156)
110	1000Genomes	NC_000009.11 - 27529316	Oct 12, 2018 (152)
111	1000Genomes_30x	NC_000009.12 - 27529318	Oct 16, 2022 (156)
112	Genome-wide autozygosity in Daghestan	NC_000009.10 - 27519316	Apr 26, 2020 (154)
113	Genetic variation in the Estonian population	NC_000009.11 - 27529316	Oct 12, 2018 (152)
114	The Danish reference pan genome	NC_000009.11 - 27529316	Apr 26, 2020 (154)
115	gnomAD - Genomes	NC_000009.12 - 27529318	Apr 26, 2021 (155)
116	HGDP-CEPH-db Supplement 1	NC_000009.10 - 27519316	Apr 26, 2020 (154)
117	HapMap	NC_000009.12 - 27529318	Apr 26, 2020 (154)
118	KOREAN population from KRGDB	NC_000009.11 - 27529316	Apr 26, 2020 (154)
119	Korean Genome Project	NC_000009.12 - 27529318	Apr 26, 2020 (154)
120	Northern Sweden	NC_000009.11 - 27529316	Jul 13, 2019 (153)
121	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000009.11 - 27529316	Apr 26, 2021 (155)
122	Qatari	NC_000009.11 - 27529316	Apr 26, 2020 (154)
123	SGDP_PRJ	NC_000009.11 - 27529316	Apr 26, 2020 (154)
124	Siberian	NC_000009.11 - 27529316	Apr 26, 2020 (154)
125	8.3KJPN	NC_000009.11 - 27529316	Apr 26, 2021 (155)
126	14KJPN	NC_000009.12 - 27529318	Oct 16, 2022 (156)
127	TopMed	NC_000009.12 - 27529318	Apr 26, 2021 (155)
128	A Vietnamese Genetic Variation Database	NC_000009.11 - 27529316	Jul 13, 2019 (153)
129	ALFA	NC_000009.12 - 27529318	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)
rs61325426	May 26, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3639408989, ss3639736846	NC_000009.9:27519315:G:A	NC_000009.12:27529317:G:A	(self)
526858, 623404, ss94035624, ss200275655, ss206774860, ss254144717, ss280166802, ss294425406, ss481834580, ss825618671, ss1397553329, ss1713102269, ss3643735380, ss3847945512	NC_000009.10:27519315:G:A	NC_000009.12:27529317:G:A	(self)
45730372, 18098536, 9212182, 26665829, 9716634, 640558, 11788402, 23842600, 6326666, 50688324, 5650754, ss224199318, ss234781110, ss241563020, ss481867140, ss482825310, ss485711796, ss561331507, ss655767532, ss783301517, ss832562869, ss833164895, ss833755723, ss986462601, ss1076231331, ss1333485243, ss1431795249, ss1583047245, ss1752773718, ss1805944091, ss1929746472, ss1971188899, ss2025584719, ss2153810312, ss2627265497, ss2634855633, ss2709616667, ss2877056802, ss3004608902, ss3348589752, ss3625981577, ss3633530748, ss3634258869, ss3635209459, ss3635936964, ss3636955927, ss3637690254, ss3638808222, ss3640916749, ss3672360288, ss3736431769, ss3744587562, ss3745509385, ss3769091219, ss3773001433, ss3786384469, ss3791605630, ss3796487307, ss3831607933, ss3839321379, ss3871825620, ss3919488435, ss3985414631, ss4017433616, ss5192719017, ss5315396193, ss5386952513, ss5509677373, ss5647195166, ss5799781881, ss5829040948, ss5976476499	NC_000009.11:27529315:G:A	NC_000009.12:27529317:G:A	(self)
59860058, 322298909, 3811059, 21938131, 69783605, 655128354, 3867411906, ss2310599324, ss3026581019, ss3649102462, ss3812249518, ss3844784205, ss3965560130, ss4817750793, ss5280292977, ss5476519988, ss5572334123, ss5735946501, ss5810465652, ss5856729811, ss5916100649	NC_000009.12:27529317:G:A	NC_000009.12:27529317:G:A	(self)
ss15540688	NT_008413.16:27519315:G:A	NC_000009.12:27529317:G:A	(self)
ss1335982, ss43888341, ss66661947, ss67891480, ss68027847, ss71592494, ss75501792, ss79288153, ss83603401, ss98232931, ss105672608, ss122942749, ss144040499, ss154479678, ss157352323, ss159654093, ss160965517, ss172426882, ss174776052	NT_008413.18:27519315:G:A	NC_000009.12:27529317:G:A	(self)
26665829, ss3919488435	NC_000009.11:27529315:G:C	NC_000009.12:27529317:G:C	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

4 citations for rs903603

PMID	Title	Author	Year	Journal
20801717	Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.	Shatunov A et al.	2010	The Lancet. Neurology
20801718	Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study.	Laaksovirta H et al.	2010	The Lancet. Neurology
22459598	Screening for C9ORF72 repeat expansion in FTLD.	Ferrari R et al.	2012	Neurobiology of aging
23587638	Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat.	Jones AR et al.	2013	Neurobiology of aging

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

rs903603