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rs6125962

From SNPedia

Orientationplus
Make rs6125962(C;C)
Make rs6125962(C;T)
Make rs6125962(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position37712660
GeneCTNNBL1
is asnp
is mentioned by
dbSNPrs6125962
ebirs6125962
HLIrs6125962
Exacrs6125962
Varsomers6125962
Maprs6125962
PheGenIrs6125962
hapmaprs6125962
1000 genomesrs6125962
hgdprs6125962
ensemblrs6125962
gopubmedrs6125962
geneviewrs6125962
scholarrs6125962
googlers6125962
pharmgkbrs6125962
gwascentralrs6125962
openSNPrs6125962
23andMers6125962
23andMe allrs6125962
SNP Nexus

SNPshotrs6125962
SNPdbers6125962
MSV3drs6125962
GWAS Ctlgrs6125962
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 27103528] Association of genetic risk factors with cognitive decline: the PATH through life project.