rs794726684

Orientation

plus

Stabilized

plus

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

Make rs794726684(-;-)

Make rs794726684(-;CA)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

67431325

Gene

HSD11B2

is a	snp
is	mentioned by
dbSNP	rs794726684
dbSNP (classic)	rs794726684
ClinGen	rs794726684
ebi	rs794726684
HLI	rs794726684
Exac	rs794726684
Gnomad	rs794726684
Varsome	rs794726684
LitVar	rs794726684
Map	rs794726684
PheGenI	rs794726684
Biobank	rs794726684
1000 genomes	rs794726684
hgdp	rs794726684
ensembl	rs794726684
geneview	rs794726684
scholar	rs794726684
google	rs794726684
pharmgkb	rs794726684
gwascentral	rs794726684
openSNP	rs794726684
23andMe	rs794726684
SNPshot	rs794726684
SNPdbe	rs794726684
MSV3d	rs794726684
GWAS Ctlg	rs794726684

Max Magnitude

0

ClinVar
Risk	rs794726684(-;-)
Alt	rs794726684(-;-)
Reference	Rs794726684(CA;CA)
Significance	Pathogenic
Disease	Apparent mineralocorticoid excess
Variation	info
Gene	HSD11B2
CLNDBN	Apparent mineralocorticoid excess
Reversed	0
HGVS	NC_000016.9:g.67465228_67465229delCA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000024128.3,