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rs201115371

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs201115371(A;A)
Make rs201115371(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position96254864
GeneHSD17B3, LOC105376162
is asnp
is mentioned by
dbSNPrs201115371
ebirs201115371
HLIrs201115371
Exacrs201115371
Varsomers201115371
Maprs201115371
PheGenIrs201115371
hapmaprs201115371
1000 genomesrs201115371
hgdprs201115371
ensemblrs201115371
gopubmedrs201115371
geneviewrs201115371
scholarrs201115371
googlers201115371
pharmgkbrs201115371
gwascentralrs201115371
openSNPrs201115371
23andMers201115371
23andMe allrs201115371
SNP Nexus

SNPshotrs201115371
SNPdbers201115371
MSV3drs201115371
GWAS Ctlgrs201115371
Max Magnitude0
ClinVar
Risk rs201115371(A;A)
Alt rs201115371(A;A)
Reference rs201115371(T;T)
Significance Pathogenic
Disease Testosterone 17-beta-dehydrogenase deficiency
Variation info
Gene HSD17B3
CLNDBN Testosterone 17-beta-dehydrogenase deficiency
Reversed 0
HGVS NC_000009.11:g.99017146T>A
CLNSRC
CLNACC RCV000190594.1,