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rs193922600

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922600(C;T)
Make rs193922600(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position120993663
GeneHNF1A
is asnp
is mentioned by
dbSNPrs193922600
ebirs193922600
HLIrs193922600
Exacrs193922600
Varsomers193922600
Maprs193922600
PheGenIrs193922600
hapmaprs193922600
1000 genomesrs193922600
hgdprs193922600
ensemblrs193922600
gopubmedrs193922600
geneviewrs193922600
scholarrs193922600
googlers193922600
pharmgkbrs193922600
gwascentralrs193922600
openSNPrs193922600
23andMers193922600
23andMe allrs193922600
SNP Nexus

SNPshotrs193922600
SNPdbers193922600
MSV3drs193922600
GWAS Ctlgrs193922600
Max Magnitude0
ClinVar
Risk rs193922600(T;T)
Alt rs193922600(T;T)
Reference rs193922600(C;C)
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.121431466C>T
CLNSRC ClinVar LabCorp
CLNACC RCV000030507.1,