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rs193922606

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922606(C;G)
Make rs193922606(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position120994322
GeneHNF1A
is asnp
is mentioned by
dbSNPrs193922606
ebirs193922606
HLIrs193922606
Exacrs193922606
Varsomers193922606
Maprs193922606
PheGenIrs193922606
hapmaprs193922606
1000 genomesrs193922606
hgdprs193922606
ensemblrs193922606
gopubmedrs193922606
geneviewrs193922606
scholarrs193922606
googlers193922606
pharmgkbrs193922606
gwascentralrs193922606
openSNPrs193922606
23andMers193922606
23andMe allrs193922606
SNP Nexus

SNPshotrs193922606
SNPdbers193922606
MSV3drs193922606
GWAS Ctlgrs193922606
Max Magnitude0
ClinVar
Risk rs193922606(A,G,T;A,G,T)
Alt rs193922606(A,G,T;A,G,T)
Reference rs193922606(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.121432125C>G
CLNSRC ClinVar LabCorp
CLNACC RCV000030514.1,