rs1053023

minus

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

Make rs1053023(A;G)

Make rs1053023(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

42313598

Gene

STAT3

is a	snp
is	mentioned by
dbSNP	rs1053023
dbSNP (classic)	rs1053023
ClinGen	rs1053023
ebi	rs1053023
HLI	rs1053023
Exac	rs1053023
Gnomad	rs1053023
Varsome	rs1053023
LitVar	rs1053023
Map	rs1053023
PheGenI	rs1053023
Biobank	rs1053023
1000 genomes	rs1053023
hgdp	rs1053023
ensembl	rs1053023
geneview	rs1053023
scholar	rs1053023
google	rs1053023
pharmgkb	rs1053023
gwascentral	rs1053023
openSNP	rs1053023
23andMe	rs1053023
SNPshot	rs1053023
SNPdbe	rs1053023
MSV3d	rs1053023
GWAS Ctlg	rs1053023

GMAF

0.2801

Max Magnitude

0

?

(A;A) (A;G) (G;G)

28

[PMID 21418178] Association of JAK-STAT pathway related genes with lymphoma risk: results of a European case-control study (EpiLymph) [PMID 18520591 ] Sequence variants in host cell factor C1 are associated with Meniere's disease.

[PMID 20059466] STAT3 polymorphisms linked with idiopathic recurrent miscarriages. [PMID 23065274] Contribution of JAK2 and STAT3 variants to the genetic susceptibility of recurrent miscarriage among Bahraini and Tunisian Arabs.

[PMID 23193966] Contribution of JAK2 and STAT3 variants to the genetic susceptibility of recurrent spontaneous miscarriage in a Tunisian population.

[PMID 25789467 ] Analysis of IL-6, STAT3 and HSPA1L Gene Polymorphisms in Anti-Tuberculosis Drug-Induced Hepatitis in a Nested Case-Control Study

ClinVar
Risk	rs1053023(G;G) rs1053023(T;T)
Alt	rs1053023(G;G) rs1053023(T;T)
Reference	Rs1053023(A;A)
Significance	Non-pathogenic
Disease	Hyper-IgE syndrome
Variation	info
Gene	STAT3
CLNDBN	Hyper-IgE syndrome
Reversed	1
HGVS	NC_000017.10:g.40465616T>C
CLNSRC
CLNACC	RCV000307257.1,

[PMID 29938592] Influence of single nucleotide polymorphisms in pri-miR-124-1 and STAT3 genes on gastric cancer susceptibility.