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rs4646038

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs4646038(A;A)
Make rs4646038(A;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position15506705
GeneCASP9
is asnp
is mentioned by
dbSNPrs4646038
ebirs4646038
HLIrs4646038
Exacrs4646038
Varsomers4646038
Maprs4646038
PheGenIrs4646038
hapmaprs4646038
1000 genomesrs4646038
hgdprs4646038
ensemblrs4646038
gopubmedrs4646038
geneviewrs4646038
scholarrs4646038
googlers4646038
pharmgkbrs4646038
gwascentralrs4646038
openSNPrs4646038
23andMers4646038
23andMe allrs4646038
SNP Nexus

SNPshotrs4646038
SNPdbers4646038
MSV3drs4646038
GWAS Ctlgrs4646038
Max Magnitude0

[PMID 19968979] Alpha-fetoprotein gene polymorphisms and risk of HCC and cirrhosis