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rs193922486

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922486(A;A)
Make rs193922486(A;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position37744664
GeneHNF1B
is asnp
is mentioned by
dbSNPrs193922486
ClinGenrs193922486
ebirs193922486
HLIrs193922486
Exacrs193922486
Varsomers193922486
Maprs193922486
PheGenIrs193922486
hapmaprs193922486
1000 genomesrs193922486
hgdprs193922486
ensemblrs193922486
gopubmedrs193922486
geneviewrs193922486
scholarrs193922486
googlers193922486
pharmgkbrs193922486
gwascentralrs193922486
openSNPrs193922486
23andMers193922486
23andMe allrs193922486
SNP Nexus

SNPshotrs193922486
SNPdbers193922486
MSV3drs193922486
GWAS Ctlgrs193922486
Max Magnitude0
ClinVar
Risk rs193922486(A;A)
Alt rs193922486(A;A)
Reference Rs193922486(T;T)
Significance Probable-Pathogenic
Disease Familial hypoplastic
Variation info
Gene HNF1B
CLNDBN Familial hypoplastic, glomerulocystic kidney
Reversed 1
HGVS NC_000017.10:g.36104655A>T
CLNSRC ClinVar
CLNACC RCV000030526.1,