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rs41511344

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in complete genomics
Make rs41511344(C;T)
Make rs41511344(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position148152550
GeneNR3C2
is asnp
is mentioned by
dbSNPrs41511344
ebirs41511344
HLIrs41511344
Exacrs41511344
Varsomers41511344
Maprs41511344
PheGenIrs41511344
hapmaprs41511344
1000 genomesrs41511344
hgdprs41511344
ensemblrs41511344
gopubmedrs41511344
geneviewrs41511344
scholarrs41511344
googlers41511344
pharmgkbrs41511344
gwascentralrs41511344
openSNPrs41511344
23andMers41511344
23andMe allrs41511344
SNP Nexus

SNPshotrs41511344
SNPdbers41511344
MSV3drs41511344
GWAS Ctlgrs41511344
Max Magnitude0
OMIM600983
Desc
Variant0005
Relatedalso


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,