rs113994135

Orientation

minus

Stabilized

minus

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

Make rs113994135(C;T)

Make rs113994135(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

42329643

Gene

STAT3

is a	snp
is	mentioned by
dbSNP	rs113994135
dbSNP (classic)	rs113994135
ClinGen	rs113994135
ebi	rs113994135
HLI	rs113994135
Exac	rs113994135
Gnomad	rs113994135
Varsome	rs113994135
LitVar	rs113994135
Map	rs113994135
PheGenI	rs113994135
Biobank	rs113994135
1000 genomes	rs113994135
hgdp	rs113994135
ensembl	rs113994135
geneview	rs113994135
scholar	rs113994135
google	rs113994135
pharmgkb	rs113994135
gwascentral	rs113994135
openSNP	rs113994135
23andMe	rs113994135
SNPshot	rs113994135
SNPdbe	rs113994135
MSV3d	rs113994135
GWAS Ctlg	rs113994135

Max Magnitude

0

OMIM	102582
Desc
Variant	0002
Related	also

ClinVar
Risk	rs113994135(T;T)
Alt	rs113994135(T;T)
Reference	Rs113994135(C;C)
Significance	Pathogenic
Disease	Hyperimmunoglobulin E syndrome not provided
Variation	info
Gene	STAT3
CLNDBN	Hyperimmunoglobulin E syndrome not provided
Reversed	1
HGVS	NC_000017.10:g.40481661G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019966.27, RCV000259784.1,