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rs137853093

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853093(A;A)
Make rs137853093(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position42787485
GeneWNK4
is asnp
is mentioned by
dbSNPrs137853093
ebirs137853093
HLIrs137853093
Exacrs137853093
Varsomers137853093
Maprs137853093
PheGenIrs137853093
hapmaprs137853093
1000 genomesrs137853093
hgdprs137853093
ensemblrs137853093
gopubmedrs137853093
geneviewrs137853093
scholarrs137853093
googlers137853093
pharmgkbrs137853093
gwascentralrs137853093
openSNPrs137853093
23andMers137853093
23andMe allrs137853093
SNP Nexus

SNPshotrs137853093
SNPdbers137853093
MSV3drs137853093
GWAS Ctlgrs137853093
Max Magnitude0
OMIM601844
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137853093(A;A)
Alt rs137853093(A;A)
Reference rs137853093(G;G)
Significance Pathogenic
Disease Pseudohypoaldosteronism type 2B
Variation info
Gene WNK4
CLNDBN Pseudohypoaldosteronism type 2B
Reversed 0
HGVS NC_000017.10:g.40939503G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008100.2,


OMIM145260
Desc
Variant
Relatedalso