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rs1057517829

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517829(C;T)
Make rs1057517829(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position31531376
GeneSRD5A2
is asnp
is mentioned by
dbSNPrs1057517829
dbSNP (old)rs1057517829
ClinGenrs1057517829
ebirs1057517829
HLIrs1057517829
Exacrs1057517829
Gnomadrs1057517829
Varsomers1057517829
Maprs1057517829
PheGenIrs1057517829
Biobankrs1057517829
1000 genomesrs1057517829
hgdprs1057517829
ensemblrs1057517829
gopubmedrs1057517829
geneviewrs1057517829
scholarrs1057517829
googlers1057517829
pharmgkbrs1057517829
gwascentralrs1057517829
openSNPrs1057517829
23andMers1057517829
23andMe allrs1057517829
SNPshotrs1057517829
SNPdbers1057517829
MSV3drs1057517829
GWAS Ctlgrs1057517829
Max Magnitude0
ClinVar
Risk rs1057517829(T;T)
Alt rs1057517829(T;T)
Reference Rs1057517829(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SRD5A2
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.31756446G>A
CLNSRC
CLNACC RCV000413891.1,