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rs193922490

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922490(C;C)
Make rs193922490(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position37739473
GeneHNF1B
is asnp
is mentioned by
dbSNPrs193922490
ebirs193922490
HLIrs193922490
Exacrs193922490
Varsomers193922490
Maprs193922490
PheGenIrs193922490
hapmaprs193922490
1000 genomesrs193922490
hgdprs193922490
ensemblrs193922490
gopubmedrs193922490
geneviewrs193922490
scholarrs193922490
googlers193922490
pharmgkbrs193922490
gwascentralrs193922490
openSNPrs193922490
23andMers193922490
23andMe allrs193922490
SNP Nexus

SNPshotrs193922490
SNPdbers193922490
MSV3drs193922490
GWAS Ctlgrs193922490
Max Magnitude0
ClinVar
Risk rs193922490(C;C)
Alt rs193922490(C;C)
Reference rs193922490(T;T)
Significance Probable-Pathogenic
Disease Familial hypoplastic
Variation info
Gene HNF1B
CLNDBN Familial hypoplastic, glomerulocystic kidney
Reversed 1
HGVS NC_000017.10:g.36099464A>G
CLNSRC ClinVar LabCorp
CLNACC RCV000030531.1,