rs41511344

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(G;G)	0	common in complete genomics

Make rs41511344(C;T)

Make rs41511344(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

148152550

Gene

NR3C2

is a	snp
is	mentioned by
dbSNP	rs41511344
dbSNP (classic)	rs41511344
ClinGen	rs41511344
ebi	rs41511344
HLI	rs41511344
Exac	rs41511344
Gnomad	rs41511344
Varsome	rs41511344
LitVar	rs41511344
Map	rs41511344
PheGenI	rs41511344
Biobank	rs41511344
1000 genomes	rs41511344
hgdp	rs41511344
ensembl	rs41511344
geneview	rs41511344
scholar	rs41511344
google	rs41511344
pharmgkb	rs41511344
gwascentral	rs41511344
openSNP	rs41511344
23andMe	rs41511344
SNPshot	rs41511344
SNPdbe	rs41511344
MSV3d	rs41511344
GWAS Ctlg	rs41511344

Max Magnitude

0

OMIM	600983
Desc
Variant	0005
Related	also

ClinVar
Risk	rs41511344(T;T)
Alt	rs41511344(T;T)
Reference	Rs41511344(C;C)
Significance	Pathogenic
Disease	Hypertension
Variation	info
Gene	NR3C2
CLNDBN	Hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy
Reversed	1
HGVS	NC_000004.11:g.149073701G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009088.2,