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rs193922582

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs193922582(-;-)
Make rs193922582(-;CT)
Make rs193922582(CT;CT)
ReferenceGRCh38 38.1/141
Chromosome12
Position120999273
GeneHNF1A
is asnp
is mentioned by
dbSNPrs193922582
ebirs193922582
HLIrs193922582
Exacrs193922582
Varsomers193922582
Maprs193922582
PheGenIrs193922582
hapmaprs193922582
1000 genomesrs193922582
hgdprs193922582
ensemblrs193922582
gopubmedrs193922582
geneviewrs193922582
scholarrs193922582
googlers193922582
pharmgkbrs193922582
gwascentralrs193922582
openSNPrs193922582
23andMers193922582
23andMe allrs193922582
SNP Nexus

SNPshotrs193922582
SNPdbers193922582
MSV3drs193922582
GWAS Ctlgrs193922582
Max Magnitude0
ClinVar
Risk rs193922582(CT;CT)
Alt rs193922582(CT;CT)
Reference rs193922582(;)
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.121437075_121437076dupCT
CLNSRC ClinVar LabCorp
CLNACC RCV000030483.1,