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rs199469626

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199469626(G;T)
Make rs199469626(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position137692320
GeneKLHL3
is asnp
is mentioned by
dbSNPrs199469626
ebirs199469626
HLIrs199469626
Exacrs199469626
Varsomers199469626
Maprs199469626
PheGenIrs199469626
hapmaprs199469626
1000 genomesrs199469626
hgdprs199469626
ensemblrs199469626
gopubmedrs199469626
geneviewrs199469626
scholarrs199469626
googlers199469626
pharmgkbrs199469626
gwascentralrs199469626
openSNPrs199469626
23andMers199469626
23andMe allrs199469626
SNP Nexus

SNPshotrs199469626
SNPdbers199469626
MSV3drs199469626
GWAS Ctlgrs199469626
Max Magnitude0
ClinVar
Risk rs199469626(T;T)
Alt rs199469626(T;T)
Reference rs199469626(G;G)
Significance Pathogenic
Disease Pseudohypoaldosteronism
Variation info
Gene KLHL3
CLNDBN Pseudohypoaldosteronism, type 2
Reversed 1
HGVS NC_000005.9:g.137028009C>A
CLNSRC ClinVar
CLNACC RCV000128505.1,