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rs193922492

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922492(G;T)
Make rs193922492(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position37731691
GeneHNF1B
is asnp
is mentioned by
dbSNPrs193922492
ebirs193922492
HLIrs193922492
Exacrs193922492
Varsomers193922492
Maprs193922492
PheGenIrs193922492
hapmaprs193922492
1000 genomesrs193922492
hgdprs193922492
ensemblrs193922492
gopubmedrs193922492
geneviewrs193922492
scholarrs193922492
googlers193922492
pharmgkbrs193922492
gwascentralrs193922492
openSNPrs193922492
23andMers193922492
23andMe allrs193922492
SNP Nexus

SNPshotrs193922492
SNPdbers193922492
MSV3drs193922492
GWAS Ctlgrs193922492
Max Magnitude0
ClinVar
Risk rs193922492(T;T)
Alt rs193922492(T;T)
Reference rs193922492(G;G)
Significance Probable-Pathogenic
Disease Familial hypoplastic
Variation info
Gene HNF1B
CLNDBN Familial hypoplastic, glomerulocystic kidney
Reversed 1
HGVS NC_000017.10:g.36091682C>A
CLNSRC ClinVar LabCorp
CLNACC RCV000030535.1,