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rs104893667

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893667(C;G)
Make rs104893667(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position31580823
GeneSRD5A2
is asnp
is mentioned by
dbSNPrs104893667
ebirs104893667
HLIrs104893667
Exacrs104893667
Varsomers104893667
Maprs104893667
PheGenIrs104893667
hapmaprs104893667
1000 genomesrs104893667
hgdprs104893667
ensemblrs104893667
gopubmedrs104893667
geneviewrs104893667
scholarrs104893667
googlers104893667
pharmgkbrs104893667
gwascentralrs104893667
openSNPrs104893667
23andMers104893667
23andMe allrs104893667
SNP Nexus

SNPshotrs104893667
SNPdbers104893667
MSV3drs104893667
GWAS Ctlgrs104893667
Max Magnitude0
OMIM607306
Desc
Variant0015
Relatedalso
ClinVar
Risk rs104893667(G;G)
Alt rs104893667(G;G)
Reference rs104893667(C;C)
Significance Pathogenic
Disease Micropenis
Variation info
Gene SRD5A2
CLNDBN Micropenis
Reversed 1
HGVS NC_000002.11:g.31805892G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000003514.5,