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rs193922737

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922737(A;G)
Make rs193922737(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position42796196
GeneWNK4
is asnp
is mentioned by
dbSNPrs193922737
dbSNP (classic)rs193922737
ClinGenrs193922737
ebirs193922737
HLIrs193922737
Exacrs193922737
Gnomadrs193922737
Varsomers193922737
LitVarrs193922737
Maprs193922737
PheGenIrs193922737
Biobankrs193922737
1000 genomesrs193922737
hgdprs193922737
ensemblrs193922737
geneviewrs193922737
scholarrs193922737
googlers193922737
pharmgkbrs193922737
gwascentralrs193922737
openSNPrs193922737
23andMers193922737
SNPshotrs193922737
SNPdbers193922737
MSV3drs193922737
GWAS Ctlgrs193922737
Max Magnitude0
ClinVar
Risk rs193922737(G;G)
Alt rs193922737(G;G)
Reference Rs193922737(A;A)
Significance Pathogenic
Disease Pseudohypoaldosteronism type 2B
Variation info
Gene WNK4
CLNDBN Pseudohypoaldosteronism type 2B
Reversed 0
HGVS NC_000017.10:g.40948214A>G
CLNSRC
CLNACC RCV000417205.1,