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rs137853095

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853095(C;T)
Make rs137853095(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position42796244
GeneWNK4
is asnp
is mentioned by
dbSNPrs137853095
ebirs137853095
HLIrs137853095
Exacrs137853095
Varsomers137853095
Maprs137853095
PheGenIrs137853095
hapmaprs137853095
1000 genomesrs137853095
hgdprs137853095
ensemblrs137853095
gopubmedrs137853095
geneviewrs137853095
scholarrs137853095
googlers137853095
pharmgkbrs137853095
gwascentralrs137853095
openSNPrs137853095
23andMers137853095
23andMe allrs137853095
SNP Nexus

SNPshotrs137853095
SNPdbers137853095
MSV3drs137853095
GWAS Ctlgrs137853095
Max Magnitude0
OMIM601844
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137853095(T;T)
Alt rs137853095(T;T)
Reference rs137853095(C;C)
Significance Pathogenic
Disease Pseudohypoaldosteronism type 2B
Variation info
Gene WNK4
CLNDBN Pseudohypoaldosteronism type 2B
Reversed 0
HGVS NC_000017.10:g.40948262C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008102.2,


OMIM145260
Desc
Variant
Relatedalso