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rs193922605

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922605(C;C)
Make rs193922605(C;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position120994253
GeneHNF1A
is asnp
is mentioned by
dbSNPrs193922605
ebirs193922605
HLIrs193922605
Exacrs193922605
Varsomers193922605
Maprs193922605
PheGenIrs193922605
hapmaprs193922605
1000 genomesrs193922605
hgdprs193922605
ensemblrs193922605
gopubmedrs193922605
geneviewrs193922605
scholarrs193922605
googlers193922605
pharmgkbrs193922605
gwascentralrs193922605
openSNPrs193922605
23andMers193922605
23andMe allrs193922605
SNP Nexus

SNPshotrs193922605
SNPdbers193922605
MSV3drs193922605
GWAS Ctlgrs193922605
Max Magnitude0
ClinVar
Risk rs193922605(C;C)
Alt rs193922605(C;C)
Reference rs193922605(T;T)
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.121432056T>C
CLNSRC ClinVar LabCorp
CLNACC RCV000030512.1,