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rs193922577

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922577(C;C)
Make rs193922577(C;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position120996698
GeneHNF1A
is asnp
is mentioned by
dbSNPrs193922577
ebirs193922577
HLIrs193922577
Exacrs193922577
Varsomers193922577
Maprs193922577
PheGenIrs193922577
hapmaprs193922577
1000 genomesrs193922577
hgdprs193922577
ensemblrs193922577
gopubmedrs193922577
geneviewrs193922577
scholarrs193922577
googlers193922577
pharmgkbrs193922577
gwascentralrs193922577
openSNPrs193922577
23andMers193922577
23andMe allrs193922577
SNP Nexus

SNPshotrs193922577
SNPdbers193922577
MSV3drs193922577
GWAS Ctlgrs193922577
Max Magnitude0
ClinVar
Risk rs193922577(C;C)
Alt rs193922577(C;C)
Reference rs193922577(T;T)
Significance Probable-Pathogenic
Disease Maturity-onset diabetes of the young
Variation info
Gene HNF1A
CLNDBN Maturity-onset diabetes of the young, type 3
Reversed 0
HGVS NC_000012.11:g.121434501T>C
CLNSRC ClinVar LabCorp
CLNACC RCV000030477.1,