rs587776843

Orientation

plus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(T;T)	0	common in clinvar

Make rs587776843(C;C)

Make rs587776843(C;T)

Reference

GRCh38 38.1/142

Chromosome

1

Position

206775286

is a	snp
is	mentioned by
dbSNP	rs587776843
dbSNP (classic)	rs587776843
ClinGen	rs587776843
ebi	rs587776843
HLI	rs587776843
Exac	rs587776843
Gnomad	rs587776843
Varsome	rs587776843
LitVar	rs587776843
Map	rs587776843
PheGenI	rs587776843
Biobank	rs587776843
1000 genomes	rs587776843
hgdp	rs587776843
ensembl	rs587776843
geneview	rs587776843
scholar	rs587776843
google	rs587776843
pharmgkb	rs587776843
gwascentral	rs587776843
openSNP	rs587776843
23andMe	rs587776843
SNPshot	rs587776843
SNPdbe	rs587776843
MSV3d	rs587776843
GWAS Ctlg	rs587776843

Max Magnitude

0

ClinVar
Risk	rs587776843(C;C) Rs587776843(T;T)
Alt	rs587776843(C;C) Rs587776843(T;T)
Reference	Rs587776843(A;A)
Significance	Pathogenic
Disease	Rheumatoid arthritis
Variation	info
Gene	IL10
CLNDBN	Rheumatoid arthritis, progression of
Reversed	1
HGVS	NC_000001.10:g.206948631T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018370.29,