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rs795659

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs795659(C;C)
Make rs795659(C;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position54179837
is asnp
is mentioned by
dbSNPrs795659
dbSNP (classic)rs795659
ClinGenrs795659
ebirs795659
HLIrs795659
Exacrs795659
Gnomadrs795659
Varsomers795659
LitVarrs795659
Maprs795659
PheGenIrs795659
Biobankrs795659
1000 genomesrs795659
hgdprs795659
ensemblrs795659
geneviewrs795659
scholarrs795659
googlers795659
pharmgkbrs795659
gwascentralrs795659
openSNPrs795659
23andMers795659
SNPshotrs795659
SNPdbers795659
MSV3drs795659
GWAS Ctlgrs795659
GMAF0.08402
Max Magnitude0
? (C;C) (C;T) (T;T) 28