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rs886039748

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs886039748(C;C)
Make rs886039748(C;T)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position31580899
GeneSRD5A2
is asnp
is mentioned by
dbSNPrs886039748
dbSNP (classic)rs886039748
ClinGenrs886039748
ebirs886039748
HLIrs886039748
Exacrs886039748
Gnomadrs886039748
Varsomers886039748
LitVarrs886039748
Maprs886039748
PheGenIrs886039748
Biobankrs886039748
1000 genomesrs886039748
hgdprs886039748
ensemblrs886039748
geneviewrs886039748
scholarrs886039748
googlers886039748
pharmgkbrs886039748
gwascentralrs886039748
openSNPrs886039748
23andMers886039748
23andMe allrs886039748
SNPshotrs886039748
SNPdbers886039748
MSV3drs886039748
GWAS Ctlgrs886039748
Max Magnitude0
ClinVar
Risk rs886039748(C;C)
Alt rs886039748(C;C)
Reference Rs886039748(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SRD5A2
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.31805968A>G
CLNSRC
CLNACC RCV000254818.1,