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rs9915936

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
(T;T) 0 common in clinvar
Make rs9915936(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position65537671
GeneAXIN2
is asnp
is mentioned by
dbSNPrs9915936
dbSNP (old)rs9915936
ClinGenrs9915936
ebirs9915936
HLIrs9915936
Exacrs9915936
Gnomadrs9915936
Varsomers9915936
Maprs9915936
PheGenIrs9915936
Biobankrs9915936
1000 genomesrs9915936
hgdprs9915936
ensemblrs9915936
gopubmedrs9915936
geneviewrs9915936
scholarrs9915936
googlers9915936
pharmgkbrs9915936
gwascentralrs9915936
openSNPrs9915936
23andMers9915936
23andMe allrs9915936
SNP Nexus

SNPshotrs9915936
SNPdbers9915936
MSV3drs9915936
GWAS Ctlgrs9915936
GMAF0.1097
Max Magnitude0

[PMID 21069480] AXIN2 polymorphism and its association with prostate cancer in a Turkish population

ClinVar
Risk Rs9915936(C;C)
Alt Rs9915936(C;C)
Reference Rs9915936(T;T)
Significance Non-pathogenic
Disease not specified Oligodontia-colorectal cancer syndrome
Variation info
Gene AXIN2
CLNDBN not specified Oligodontia-colorectal cancer syndrome
Reversed 0
HGVS NC_000017.10:g.63533789T>C
CLNSRC
CLNACC RCV000250428.1, RCV000305836.1,