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rs139332887

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs139332887(A;A)
Make rs139332887(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position27239731
GeneCAD
is asnp
is mentioned by
dbSNPrs139332887
dbSNP (old)rs139332887
ClinGenrs139332887
ebirs139332887
HLIrs139332887
Exacrs139332887
Gnomadrs139332887
Varsomers139332887
Maprs139332887
PheGenIrs139332887
Biobankrs139332887
1000 genomesrs139332887
hgdprs139332887
ensemblrs139332887
gopubmedrs139332887
geneviewrs139332887
scholarrs139332887
googlers139332887
pharmgkbrs139332887
gwascentralrs139332887
openSNPrs139332887
23andMers139332887
23andMe allrs139332887
SNPshotrs139332887
SNPdbers139332887
MSV3drs139332887
GWAS Ctlgrs139332887
Max Magnitude0
ClinVar
Risk rs139332887(A;A)
Alt rs139332887(A;A)
Reference Rs139332887(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CAD
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.27462599G>A
CLNSRC
CLNACC RCV000485191.1,