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rs193922594

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs193922594(-;-)
Make rs193922594(-;G)
Make rs193922594(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position120979081
GeneHNF1A
is asnp
is mentioned by
dbSNPrs193922594
ebirs193922594
HLIrs193922594
Exacrs193922594
Varsomers193922594
Maprs193922594
PheGenIrs193922594
hapmaprs193922594
1000 genomesrs193922594
hgdprs193922594
ensemblrs193922594
gopubmedrs193922594
geneviewrs193922594
scholarrs193922594
googlers193922594
pharmgkbrs193922594
gwascentralrs193922594
openSNPrs193922594
23andMers193922594
23andMe allrs193922594
SNP Nexus

SNPshotrs193922594
SNPdbers193922594
MSV3drs193922594
GWAS Ctlgrs193922594
Max Magnitude0
ClinVar
Risk rs193922594(G;G)
Alt rs193922594(G;G)
Reference rs193922594(;)
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.121416884dupG
CLNSRC ClinVar LabCorp
CLNACC RCV000030498.1,