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rs368386747

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs368386747(C;C)
Make rs368386747(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position31533671
GeneSRD5A2
is asnp
is mentioned by
dbSNPrs368386747
dbSNP (classic)rs368386747
ClinGenrs368386747
ebirs368386747
HLIrs368386747
Exacrs368386747
Gnomadrs368386747
Varsomers368386747
LitVarrs368386747
Maprs368386747
PheGenIrs368386747
Biobankrs368386747
1000 genomesrs368386747
hgdprs368386747
ensemblrs368386747
geneviewrs368386747
scholarrs368386747
googlers368386747
pharmgkbrs368386747
gwascentralrs368386747
openSNPrs368386747
23andMers368386747
23andMe allrs368386747
SNPshotrs368386747
SNPdbers368386747
MSV3drs368386747
GWAS Ctlgrs368386747
Max Magnitude0
ClinVar
Risk rs368386747(C;C)
Alt rs368386747(C;C)
Reference Rs368386747(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SRD5A2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.31758741T>C
CLNSRC
CLNACC RCV000413020.1,