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rs193922491

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922491(C;T)
Make rs193922491(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position37733663
GeneHNF1B
is asnp
is mentioned by
dbSNPrs193922491
ebirs193922491
HLIrs193922491
Exacrs193922491
Varsomers193922491
Maprs193922491
PheGenIrs193922491
hapmaprs193922491
1000 genomesrs193922491
hgdprs193922491
ensemblrs193922491
gopubmedrs193922491
geneviewrs193922491
scholarrs193922491
googlers193922491
pharmgkbrs193922491
gwascentralrs193922491
openSNPrs193922491
23andMers193922491
23andMe allrs193922491
SNP Nexus

SNPshotrs193922491
SNPdbers193922491
MSV3drs193922491
GWAS Ctlgrs193922491
Max Magnitude0
ClinVar
Risk rs193922491(T;T)
Alt rs193922491(T;T)
Reference rs193922491(C;C)
Significance Probable-Pathogenic
Disease Familial hypoplastic
Variation info
Gene HNF1B
CLNDBN Familial hypoplastic, glomerulocystic kidney
Reversed 1
HGVS NC_000017.10:g.36093656G>A
CLNSRC ClinVar LabCorp
CLNACC RCV000030532.1,