rs869312889

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs869312889(C;T)

Make rs869312889(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

42322395

Gene

STAT3

is a	snp
is	mentioned by
dbSNP	rs869312889
dbSNP (classic)	rs869312889
ClinGen	rs869312889
ebi	rs869312889
HLI	rs869312889
Exac	rs869312889
Gnomad	rs869312889
Varsome	rs869312889
LitVar	rs869312889
Map	rs869312889
PheGenI	rs869312889
Biobank	rs869312889
1000 genomes	rs869312889
hgdp	rs869312889
ensembl	rs869312889
geneview	rs869312889
scholar	rs869312889
google	rs869312889
pharmgkb	rs869312889
gwascentral	rs869312889
openSNP	rs869312889
23andMe	rs869312889
SNPshot	rs869312889
SNPdbe	rs869312889
MSV3d	rs869312889
GWAS Ctlg	rs869312889

Max Magnitude

0

ClinVar
Risk	rs869312889(T;T)
Alt	rs869312889(T;T)
Reference	Rs869312889(C;C)
Significance	Pathogenic
Disease	Autoimmune disease
Variation	info
Gene	STAT3
CLNDBN	Autoimmune disease, multisystem, infantile-onset, 1
Reversed	1
HGVS	NC_000017.10:g.40474413G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000210428.4,