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

rs199469631

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199469631(A;A)
Make rs199469631(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position137637320
GeneKLHL3
is asnp
is mentioned by
dbSNPrs199469631
ebirs199469631
HLIrs199469631
Exacrs199469631
Varsomers199469631
Maprs199469631
PheGenIrs199469631
hapmaprs199469631
1000 genomesrs199469631
hgdprs199469631
ensemblrs199469631
gopubmedrs199469631
geneviewrs199469631
scholarrs199469631
googlers199469631
pharmgkbrs199469631
gwascentralrs199469631
openSNPrs199469631
23andMers199469631
23andMe allrs199469631
SNP Nexus

SNPshotrs199469631
SNPdbers199469631
MSV3drs199469631
GWAS Ctlgrs199469631
Max Magnitude0
ClinVar
Risk rs199469631(A;A)
Alt rs199469631(A;A)
Reference rs199469631(G;G)
Significance Pathogenic
Disease Pseudohypoaldosteronism
Variation info
Gene KLHL3
CLNDBN Pseudohypoaldosteronism, type 2
Reversed 1
HGVS NC_000005.9:g.136973009C>T
CLNSRC ClinVar
CLNACC RCV000128522.1,