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rs4531631

From SNPedia

Orientationplus
Make rs4531631(A;A)
Make rs4531631(A;G)
Make rs4531631(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position42560995
GeneTNFSF11
is asnp
is mentioned by
dbSNPrs4531631
ebirs4531631
HLIrs4531631
Exacrs4531631
Varsomers4531631
Maprs4531631
PheGenIrs4531631
hapmaprs4531631
1000 genomesrs4531631
hgdprs4531631
ensemblrs4531631
gopubmedrs4531631
geneviewrs4531631
scholarrs4531631
googlers4531631
pharmgkbrs4531631
gwascentralrs4531631
openSNPrs4531631
23andMers4531631
23andMe allrs4531631
SNP Nexus

SNPshotrs4531631
SNPdbers4531631
MSV3drs4531631
GWAS Ctlgrs4531631
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 27567908] Association Between Single Nucleotide Polymorphisms in NFATC1 Signaling Pathway Genes and Susceptibility to Congenital Heart Disease in the Chinese Population.