rs869312892

Orientation

minus

Stabilized

minus

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

Make rs869312892(C;T)

Make rs869312892(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

42316899

Gene

STAT3

is a	snp
is	mentioned by
dbSNP	rs869312892
dbSNP (classic)	rs869312892
ClinGen	rs869312892
ebi	rs869312892
HLI	rs869312892
Exac	rs869312892
Gnomad	rs869312892
Varsome	rs869312892
LitVar	rs869312892
Map	rs869312892
PheGenI	rs869312892
Biobank	rs869312892
1000 genomes	rs869312892
hgdp	rs869312892
ensembl	rs869312892
geneview	rs869312892
scholar	rs869312892
google	rs869312892
pharmgkb	rs869312892
gwascentral	rs869312892
openSNP	rs869312892
23andMe	rs869312892
SNPshot	rs869312892
SNPdbe	rs869312892
MSV3d	rs869312892
GWAS Ctlg	rs869312892

Max Magnitude

0

ClinVar
Risk	rs869312892(T;T)
Alt	rs869312892(T;T)
Reference	Rs869312892(C;C)
Significance	Pathogenic
Disease	Autoimmune disease not provided
Variation	info
Gene	STAT3
CLNDBN	Autoimmune disease, multisystem, infantile-onset, 1 not provided
Reversed	1
HGVS	NC_000017.10:g.40468917G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000210415.4, RCV000224259.1,