rs786200876

Orientation

plus

Stabilized

plus

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

Make rs786200876(-;-)

Make rs786200876(-;AG)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

30985703

Gene

HSD3B7

is a	snp
is	mentioned by
dbSNP	rs786200876
dbSNP (classic)	rs786200876
ClinGen	rs786200876
ebi	rs786200876
HLI	rs786200876
Exac	rs786200876
Gnomad	rs786200876
Varsome	rs786200876
LitVar	rs786200876
Map	rs786200876
PheGenI	rs786200876
Biobank	rs786200876
1000 genomes	rs786200876
hgdp	rs786200876
ensembl	rs786200876
geneview	rs786200876
scholar	rs786200876
google	rs786200876
pharmgkb	rs786200876
gwascentral	rs786200876
openSNP	rs786200876
23andMe	rs786200876
SNPshot	rs786200876
SNPdbe	rs786200876
MSV3d	rs786200876
GWAS Ctlg	rs786200876

Max Magnitude

0

ClinVar
Risk	rs786200876(-;-)
Alt	rs786200876(-;-)
Reference	Rs786200876(AG;AG)
Significance	Pathogenic
Disease	Bile acid synthesis defect
Variation	info
Gene	HSD3B7
CLNDBN	Bile acid synthesis defect, congenital, 1
Reversed	0
HGVS	NC_000016.9:g.30997024_30997025delAG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003019.3,