Have questions? Visit https://www.reddit.com/r/SNPedia

rs199469651

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199469651(G;G)
Make rs199469651(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position224503834
GeneCUL3
is asnp
is mentioned by
dbSNPrs199469651
ebirs199469651
HLIrs199469651
Exacrs199469651
Varsomers199469651
Maprs199469651
PheGenIrs199469651
hapmaprs199469651
1000 genomesrs199469651
hgdprs199469651
ensemblrs199469651
gopubmedrs199469651
geneviewrs199469651
scholarrs199469651
googlers199469651
pharmgkbrs199469651
gwascentralrs199469651
openSNPrs199469651
23andMers199469651
23andMe allrs199469651
SNP Nexus

SNPshotrs199469651
SNPdbers199469651
MSV3drs199469651
GWAS Ctlgrs199469651
Max Magnitude0
ClinVar
Risk rs199469651(G;G)
Alt rs199469651(G;G)
Reference rs199469651(T;T)
Significance Pathogenic
Disease Pseudohypoaldosteronism
Variation info
Gene CUL3
CLNDBN Pseudohypoaldosteronism, type 2
Reversed 1
HGVS NC_000002.11:g.225368551A>C
CLNSRC ClinVar
CLNACC RCV000128486.1,