rs397514766

Orientation

minus

Stabilized

minus

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

Make rs397514766(C;T)

Make rs397514766(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

42329621

Gene

STAT3

is a	snp
is	mentioned by
dbSNP	rs397514766
dbSNP (classic)	rs397514766
ClinGen	rs397514766
ebi	rs397514766
HLI	rs397514766
Exac	rs397514766
Gnomad	rs397514766
Varsome	rs397514766
LitVar	rs397514766
Map	rs397514766
PheGenI	rs397514766
Biobank	rs397514766
1000 genomes	rs397514766
hgdp	rs397514766
ensembl	rs397514766
geneview	rs397514766
scholar	rs397514766
google	rs397514766
pharmgkb	rs397514766
gwascentral	rs397514766
openSNP	rs397514766
23andMe	rs397514766
SNPshot	rs397514766
SNPdbe	rs397514766
MSV3d	rs397514766
GWAS Ctlg	rs397514766

Max Magnitude

0

ClinVar
Risk	rs397514766(T;T)
Alt	rs397514766(T;T)
Reference	Rs397514766(C;C)
Significance	Pathogenic
Disease	Hyperimmunoglobulin E syndrome
Variation	info
Gene	STAT3
CLNDBN	Hyperimmunoglobulin E syndrome
Reversed	1
HGVS	NC_000017.10:g.40481639G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000054835.28,