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rs1377638

From SNPedia

Orientationplus
Stabilizedplus
Make rs1377638(C;C)
Make rs1377638(C;T)
Make rs1377638(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position5153392
is asnp
is mentioned by
dbSNPrs1377638
dbSNP (classic)rs1377638
ClinGenrs1377638
ebirs1377638
HLIrs1377638
Exacrs1377638
Gnomadrs1377638
Varsomers1377638
LitVarrs1377638
Maprs1377638
PheGenIrs1377638
Biobankrs1377638
1000 genomesrs1377638
hgdprs1377638
ensemblrs1377638
geneviewrs1377638
scholarrs1377638
googlers1377638
pharmgkbrs1377638
gwascentralrs1377638
openSNPrs1377638
23andMers1377638
SNPshotrs1377638
SNPdbers1377638
MSV3drs1377638
GWAS Ctlgrs1377638
GMAF0.208
Max Magnitude0
? (C;C) (C;T) (T;T) 28


Mentioned in retracted [PMID 20595579]