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rs193922589

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922589(A;G)
Make rs193922589(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position120999604
GeneHNF1A
is asnp
is mentioned by
dbSNPrs193922589
ebirs193922589
HLIrs193922589
Exacrs193922589
Varsomers193922589
Maprs193922589
PheGenIrs193922589
hapmaprs193922589
1000 genomesrs193922589
hgdprs193922589
ensemblrs193922589
gopubmedrs193922589
geneviewrs193922589
scholarrs193922589
googlers193922589
pharmgkbrs193922589
gwascentralrs193922589
openSNPrs193922589
23andMers193922589
23andMe allrs193922589
SNP Nexus

SNPshotrs193922589
SNPdbers193922589
MSV3drs193922589
GWAS Ctlgrs193922589
Max Magnitude0
ClinVar
Risk rs193922589(G;G)
Alt rs193922589(G;G)
Reference rs193922589(A;A)
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.121437407A>G
CLNSRC ClinVar LabCorp
CLNACC RCV000030491.1,