rs387907117

Orientation

plus

Stabilized

plus

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

Make rs387907117(C;C)

Make rs387907117(C;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

67436797

Gene

HSD11B2

is a	snp
is	mentioned by
dbSNP	rs387907117
dbSNP (classic)	rs387907117
ClinGen	rs387907117
ebi	rs387907117
HLI	rs387907117
Exac	rs387907117
Gnomad	rs387907117
Varsome	rs387907117
LitVar	rs387907117
Map	rs387907117
PheGenI	rs387907117
Biobank	rs387907117
1000 genomes	rs387907117
hgdp	rs387907117
ensembl	rs387907117
geneview	rs387907117
scholar	rs387907117
google	rs387907117
pharmgkb	rs387907117
gwascentral	rs387907117
openSNP	rs387907117
23andMe	rs387907117
SNPshot	rs387907117
SNPdbe	rs387907117
MSV3d	rs387907117
GWAS Ctlg	rs387907117

Max Magnitude

0

ClinVar
Risk	rs387907117(C;C)
Alt	rs387907117(C;C)
Reference	Rs387907117(T;T)
Significance	Pathogenic
Disease	Apparent mineralocorticoid excess
Variation	info
Gene	HSD11B2
CLNDBN	Apparent mineralocorticoid excess
Reversed	0
HGVS	NC_000016.9:g.67470700T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000024127.5,