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rs199469637

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199469637(C;T)
Make rs199469637(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position137692381
GeneKLHL3
is asnp
is mentioned by
dbSNPrs199469637
ebirs199469637
HLIrs199469637
Exacrs199469637
Varsomers199469637
Maprs199469637
PheGenIrs199469637
hapmaprs199469637
1000 genomesrs199469637
hgdprs199469637
ensemblrs199469637
gopubmedrs199469637
geneviewrs199469637
scholarrs199469637
googlers199469637
pharmgkbrs199469637
gwascentralrs199469637
openSNPrs199469637
23andMers199469637
23andMe allrs199469637
SNP Nexus

SNPshotrs199469637
SNPdbers199469637
MSV3drs199469637
GWAS Ctlgrs199469637
Max Magnitude0
ClinVar
Risk rs199469637(T;T)
Alt rs199469637(T;T)
Reference rs199469637(C;C)
Significance Pathogenic
Disease Pseudohypoaldosteronism
Variation info
Gene KLHL3
CLNDBN Pseudohypoaldosteronism, type 2
Reversed 1
HGVS NC_000005.9:g.137028070G>A
CLNSRC ClinVar
CLNACC RCV000128512.1,