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rs1764391

From SNPedia

Orientationplus
Stabilizedplus
Make rs1764391(C;C)
Make rs1764391(C;T)
Make rs1764391(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position34795168
GeneGJA4
is asnp
is mentioned by
dbSNPrs1764391
ebirs1764391
HLIrs1764391
Exacrs1764391
Varsomers1764391
Maprs1764391
PheGenIrs1764391
hapmaprs1764391
1000 genomesrs1764391
hgdprs1764391
ensemblrs1764391
gopubmedrs1764391
geneviewrs1764391
scholarrs1764391
googlers1764391
pharmgkbrs1764391
gwascentralrs1764391
openSNPrs1764391
23andMers1764391
23andMe allrs1764391
SNP Nexus

SNPshotrs1764391
SNPdbers1764391
MSV3drs1764391
GWAS Ctlgrs1764391
GMAF0.3333
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 23906684] Genetic associations with coronary heart disease: Meta-analyses of 12 candidate genetic variants


[PMID 18182569OA-icon.png] Pharmacogenetics of minimal residual disease response in children with B-precursor acute lymphoblastic leukemia: a report from the Children's Oncology Group.


[PMID 22305353] Lack of association between a functional genetic variant of connexin 37 and ischemic stroke in a Taiwanese population.


[PMID 24773516] Cx37 C1019T Polymorphism May Contribute to the Pathogenesis of Coronary Heart Disease


[PMID 26656196] Analysis of Connexin37 gene C1019T polymorphism and PCOS susceptibility in South Indian population: case-control study.