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rs964293

From SNPedia

Orientationminus
Make rs964293(G;G)
Make rs964293(G;T)
Make rs964293(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position54200178
is asnp
is mentioned by
dbSNPrs964293
ebirs964293
HLIrs964293
Exacrs964293
Varsomers964293
Maprs964293
PheGenIrs964293
hapmaprs964293
1000 genomesrs964293
hgdprs964293
ensemblrs964293
gopubmedrs964293
geneviewrs964293
scholarrs964293
googlers964293
pharmgkbrs964293
gwascentralrs964293
openSNPrs964293
23andMers964293
23andMe allrs964293
SNP Nexus

SNPshotrs964293
SNPdbers964293
MSV3drs964293
GWAS Ctlgrs964293
Max Magnitude
? (G;G) (G;T) (T;T) 28
[PMID 26766742] CYP24A1 variant rs964293 modifies the association between use of combination hormone replacement therapy and colorectal cancer risk.