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rs1053023

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1053023(A;G)
Make rs1053023(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position42313598
GeneSTAT3
is asnp
is mentioned by
dbSNPrs1053023
dbSNP (classic)rs1053023
ClinGenrs1053023
ebirs1053023
HLIrs1053023
Exacrs1053023
Gnomadrs1053023
Varsomers1053023
LitVarrs1053023
Maprs1053023
PheGenIrs1053023
Biobankrs1053023
1000 genomesrs1053023
hgdprs1053023
ensemblrs1053023
geneviewrs1053023
scholarrs1053023
googlers1053023
pharmgkbrs1053023
gwascentralrs1053023
openSNPrs1053023
23andMers1053023
SNPshotrs1053023
SNPdbers1053023
MSV3drs1053023
GWAS Ctlgrs1053023
GMAF0.2801
Max Magnitude0
? (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 18520591OA-icon.png] 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 25789467OA-icon.png] 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.