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rs8177441

From SNPedia

Orientationplus
Make rs8177441(C;C)
Make rs8177441(C;G)
Make rs8177441(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position151026433
GeneGPX3
is asnp
is mentioned by
dbSNPrs8177441
ebirs8177441
HLIrs8177441
Exacrs8177441
Varsomers8177441
Maprs8177441
PheGenIrs8177441
hapmaprs8177441
1000 genomesrs8177441
hgdprs8177441
ensemblrs8177441
gopubmedrs8177441
geneviewrs8177441
scholarrs8177441
googlers8177441
pharmgkbrs8177441
gwascentralrs8177441
openSNPrs8177441
23andMers8177441
23andMe allrs8177441
SNP Nexus

SNPshotrs8177441
SNPdbers8177441
MSV3drs8177441
GWAS Ctlgrs8177441
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 26612412] A Three-Way Interaction among Maternal and Fetal Variants Contributing to Congenital Heart Defects.