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rs747329682

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs747329682(A;A)
Make rs747329682(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position96298423
GeneHSD17B3
is asnp
is mentioned by
dbSNPrs747329682
ebirs747329682
HLIrs747329682
Exacrs747329682
Varsomers747329682
Maprs747329682
PheGenIrs747329682
hapmaprs747329682
1000 genomesrs747329682
hgdprs747329682
ensemblrs747329682
gopubmedrs747329682
geneviewrs747329682
scholarrs747329682
googlers747329682
pharmgkbrs747329682
gwascentralrs747329682
openSNPrs747329682
23andMers747329682
23andMe allrs747329682
SNP Nexus

SNPshotrs747329682
SNPdbers747329682
MSV3drs747329682
GWAS Ctlgrs747329682
Max Magnitude0
ClinVar
Risk rs747329682(A;A)
Alt rs747329682(A;A)
Reference rs747329682(G;G)
Significance Probable-Pathogenic
Disease Testosterone 17-beta-dehydrogenase deficiency
Variation info
Gene HSD17B3
CLNDBN Testosterone 17-beta-dehydrogenase deficiency
Reversed 0
HGVS NC_000009.11:g.99060705G>A
CLNSRC
CLNACC RCV000198988.1,