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rs193922487

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922487(A;A)
Make rs193922487(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position37744541
GeneHNF1B
is asnp
is mentioned by
dbSNPrs193922487
ebirs193922487
HLIrs193922487
Exacrs193922487
Varsomers193922487
Maprs193922487
PheGenIrs193922487
hapmaprs193922487
1000 genomesrs193922487
hgdprs193922487
ensemblrs193922487
gopubmedrs193922487
geneviewrs193922487
scholarrs193922487
googlers193922487
pharmgkbrs193922487
gwascentralrs193922487
openSNPrs193922487
23andMers193922487
23andMe allrs193922487
SNP Nexus

SNPshotrs193922487
SNPdbers193922487
MSV3drs193922487
GWAS Ctlgrs193922487
Max Magnitude0
ClinVar
Risk rs193922487(A;A)
Alt rs193922487(A;A)
Reference rs193922487(G;G)
Significance Probable-Pathogenic
Disease Familial hypoplastic
Variation info
Gene HNF1B
CLNDBN Familial hypoplastic, glomerulocystic kidney
Reversed 1
HGVS NC_000017.10:g.36104532C>T
CLNSRC ClinVar LabCorp
CLNACC RCV000030527.1,