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rs193922603

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922603(G;T)
Make rs193922603(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position120994184
GeneHNF1A
is asnp
is mentioned by
dbSNPrs193922603
ebirs193922603
HLIrs193922603
Exacrs193922603
Varsomers193922603
Maprs193922603
PheGenIrs193922603
hapmaprs193922603
1000 genomesrs193922603
hgdprs193922603
ensemblrs193922603
gopubmedrs193922603
geneviewrs193922603
scholarrs193922603
googlers193922603
pharmgkbrs193922603
gwascentralrs193922603
openSNPrs193922603
23andMers193922603
23andMe allrs193922603
SNP Nexus

SNPshotrs193922603
SNPdbers193922603
MSV3drs193922603
GWAS Ctlgrs193922603
Max Magnitude0
ClinVar
Risk rs193922603(T;T)
Alt rs193922603(T;T)
Reference rs193922603(G;G)
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.121431987G>T
CLNSRC ClinVar LabCorp
CLNACC RCV000030510.1,