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rs137853092

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853092(C;G)
Make rs137853092(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position42787494
GeneWNK4
is asnp
is mentioned by
dbSNPrs137853092
ebirs137853092
HLIrs137853092
Exacrs137853092
Varsomers137853092
Maprs137853092
PheGenIrs137853092
hapmaprs137853092
1000 genomesrs137853092
hgdprs137853092
ensemblrs137853092
gopubmedrs137853092
geneviewrs137853092
scholarrs137853092
googlers137853092
pharmgkbrs137853092
gwascentralrs137853092
openSNPrs137853092
23andMers137853092
23andMe allrs137853092
SNP Nexus

SNPshotrs137853092
SNPdbers137853092
MSV3drs137853092
GWAS Ctlgrs137853092
Max Magnitude0
OMIM601844
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137853092(G;G)
Alt rs137853092(G;G)
Reference Rs137853092(C;C)
Significance Pathogenic
Disease Pseudohypoaldosteronism type 2B
Variation info
Gene WNK4
CLNDBN Pseudohypoaldosteronism type 2B
Reversed 0
HGVS NC_000017.10:g.40939512C>G
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000008099.2,


OMIM145260
Desc
Variant
Relatedalso