rs786205627

Orientation

plus

Stabilized

plus

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

Make rs786205627(-;-)

Make rs786205627(-;T)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

30987004

Gene

HSD3B7

is a	snp
is	mentioned by
dbSNP	rs786205627
dbSNP (classic)	rs786205627
ClinGen	rs786205627
ebi	rs786205627
HLI	rs786205627
Exac	rs786205627
Gnomad	rs786205627
Varsome	rs786205627
LitVar	rs786205627
Map	rs786205627
PheGenI	rs786205627
Biobank	rs786205627
1000 genomes	rs786205627
hgdp	rs786205627
ensembl	rs786205627
geneview	rs786205627
scholar	rs786205627
google	rs786205627
pharmgkb	rs786205627
gwascentral	rs786205627
openSNP	rs786205627
23andMe	rs786205627
SNPshot	rs786205627
SNPdbe	rs786205627
MSV3d	rs786205627
GWAS Ctlg	rs786205627

Max Magnitude

0

ClinVar
Risk	rs786205627(-;-)
Alt	rs786205627(-;-)
Reference	Rs786205627(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	HSD3B7
CLNDBN	not provided
Reversed	0
HGVS	NC_000016.9:g.30998325delT
CLNSRC
CLNACC	RCV000171481.1,