rs747329682

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs747329682(A;A)

Make rs747329682(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

96298423

Gene

HSD17B3

is a	snp
is	mentioned by
dbSNP	rs747329682
dbSNP (classic)	rs747329682
ClinGen	rs747329682
ebi	rs747329682
HLI	rs747329682
Exac	rs747329682
Gnomad	rs747329682
Varsome	rs747329682
LitVar	rs747329682
Map	rs747329682
PheGenI	rs747329682
Biobank	rs747329682
1000 genomes	rs747329682
hgdp	rs747329682
ensembl	rs747329682
geneview	rs747329682
scholar	rs747329682
google	rs747329682
pharmgkb	rs747329682
gwascentral	rs747329682
openSNP	rs747329682
23andMe	rs747329682
SNPshot	rs747329682
SNPdbe	rs747329682
MSV3d	rs747329682
GWAS Ctlg	rs747329682

Max Magnitude

0

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	UniProtKB (protein)
CLNACC	RCV000198988.1,