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rs193922493

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922493(A;G)
Make rs193922493(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position37731678
GeneHNF1B
is asnp
is mentioned by
dbSNPrs193922493
ebirs193922493
HLIrs193922493
Exacrs193922493
Varsomers193922493
Maprs193922493
PheGenIrs193922493
hapmaprs193922493
1000 genomesrs193922493
hgdprs193922493
ensemblrs193922493
gopubmedrs193922493
geneviewrs193922493
scholarrs193922493
googlers193922493
pharmgkbrs193922493
gwascentralrs193922493
openSNPrs193922493
23andMers193922493
23andMe allrs193922493
SNP Nexus

SNPshotrs193922493
SNPdbers193922493
MSV3drs193922493
GWAS Ctlgrs193922493
Max Magnitude0
ClinVar
Risk rs193922493(G;G)
Alt rs193922493(G;G)
Reference rs193922493(A;A)
Significance Probable-Pathogenic
Disease Familial hypoplastic
Variation info
Gene HNF1B
CLNDBN Familial hypoplastic, glomerulocystic kidney
Reversed 1
HGVS NC_000017.10:g.36091669T>C
CLNSRC ClinVar LabCorp
CLNACC RCV000030537.1,