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

rs137853094

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137853094(A;C)
Make rs137853094(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position42787492
GeneWNK4
is asnp
is mentioned by
dbSNPrs137853094
ebirs137853094
HLIrs137853094
Exacrs137853094
Varsomers137853094
Maprs137853094
PheGenIrs137853094
hapmaprs137853094
1000 genomesrs137853094
hgdprs137853094
ensemblrs137853094
gopubmedrs137853094
geneviewrs137853094
scholarrs137853094
googlers137853094
pharmgkbrs137853094
gwascentralrs137853094
openSNPrs137853094
23andMers137853094
23andMe allrs137853094
SNP Nexus

SNPshotrs137853094
SNPdbers137853094
MSV3drs137853094
GWAS Ctlgrs137853094
Max Magnitude0
OMIM601844
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137853094(C;C)
Alt rs137853094(C;C)
Reference rs137853094(A;A)
Significance Pathogenic
Disease Pseudohypoaldosteronism type 2B
Variation info
Gene WNK4
CLNDBN Pseudohypoaldosteronism type 2B
Reversed 0
HGVS NC_000017.10:g.40939510A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000008101.2,


OMIM145260
Desc
Variant
Relatedalso