rs10985112

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs10985112(A;A)

Make rs10985112(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

120969130

Gene

C5

is a	snp
is	mentioned by
dbSNP	rs10985112
dbSNP (classic)	rs10985112
ClinGen	rs10985112
ebi	rs10985112
HLI	rs10985112
Exac	rs10985112
Gnomad	rs10985112
Varsome	rs10985112
LitVar	rs10985112
Map	rs10985112
PheGenI	rs10985112
Biobank	rs10985112
1000 genomes	rs10985112
hgdp	rs10985112
ensembl	rs10985112
geneview	rs10985112
scholar	rs10985112
google	rs10985112
pharmgkb	rs10985112
gwascentral	rs10985112
openSNP	rs10985112
23andMe	rs10985112
SNPshot	rs10985112
SNPdbe	rs10985112
MSV3d	rs10985112
GWAS Ctlg	rs10985112

GMAF

0.1552

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

Rs10985112
PubMed	[PMID 17880261]
Affy Probeset	SNP_A-4241423
Affy Orientation	same
On GW 5.0	1
Alleles A/B	A/G
Ancestral	A
Population	Caucasian
Allele	A
Case Freq.	0.1
Control Freq.	0.07
Odds Ratio Het
Odds Ratio Hom
Odds Ratio All	1.57
Disease	Rheumatoid Arthritis (RA)

rs10985112 increases susceptibility to Rheumatoid Arthritis 1.57 times for carriers of the A allele [PMID 17880261]

[PMID 20018075] Genome-wide association study of rheumatoid arthritis by a score test based on wavelet transformation.

ClinVar
Risk	rs10985112(A;A)
Alt	rs10985112(A;A)
Reference	Rs10985112(G;G)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	C5
CLNDBN	not specified
Reversed	0
HGVS	NC_000009.11:g.123731408G>A
CLNSRC
CLNACC	RCV000456091.1,