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rs964293

From SNPedia

Orientationminus
Stabilizedminus
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
dbSNP (classic)rs964293
ClinGenrs964293
ebirs964293
HLIrs964293
Exacrs964293
Gnomadrs964293
Varsomers964293
LitVarrs964293
Maprs964293
PheGenIrs964293
Biobankrs964293
1000 genomesrs964293
hgdprs964293
ensemblrs964293
geneviewrs964293
scholarrs964293
googlers964293
pharmgkbrs964293
gwascentralrs964293
openSNPrs964293
23andMers964293
SNPshotrs964293
SNPdbers964293
MSV3drs964293
GWAS Ctlgrs964293
Max Magnitude0
? (G;G) (G;T) (T;T) 28


[PMID 26766742OA-icon.png] CYP24A1 variant rs964293 modifies the association between use of combination hormone replacement therapy and colorectal cancer risk.