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rs193922736

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922736(C;C)
Make rs193922736(C;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position42787491
GeneWNK4
is asnp
is mentioned by
dbSNPrs193922736
dbSNP (classic)rs193922736
ClinGenrs193922736
ebirs193922736
HLIrs193922736
Exacrs193922736
Gnomadrs193922736
Varsomers193922736
LitVarrs193922736
Maprs193922736
PheGenIrs193922736
Biobankrs193922736
1000 genomesrs193922736
hgdprs193922736
ensemblrs193922736
geneviewrs193922736
scholarrs193922736
googlers193922736
pharmgkbrs193922736
gwascentralrs193922736
openSNPrs193922736
23andMers193922736
SNPshotrs193922736
SNPdbers193922736
MSV3drs193922736
GWAS Ctlgrs193922736
Max Magnitude0
ClinVar
Risk rs193922736(C;C)
Alt rs193922736(C;C)
Reference Rs193922736(G;G)
Significance Pathogenic
Disease Pseudohypoaldosteronism type 2B
Variation info
Gene WNK4
CLNDBN Pseudohypoaldosteronism type 2B
Reversed 0
HGVS NC_000017.10:g.40939509G>C
CLNSRC
CLNACC RCV000417204.1,