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rs193922474

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922474(C;C)
Make rs193922474(C;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position44414633
GeneHNF4A
is asnp
is mentioned by
dbSNPrs193922474
ebirs193922474
HLIrs193922474
Exacrs193922474
Varsomers193922474
Maprs193922474
PheGenIrs193922474
hapmaprs193922474
1000 genomesrs193922474
hgdprs193922474
ensemblrs193922474
gopubmedrs193922474
geneviewrs193922474
scholarrs193922474
googlers193922474
pharmgkbrs193922474
gwascentralrs193922474
openSNPrs193922474
23andMers193922474
23andMe allrs193922474
SNP Nexus

SNPshotrs193922474
SNPdbers193922474
MSV3drs193922474
GWAS Ctlgrs193922474
Max Magnitude0
ClinVar
Risk rs193922474(C;C)
Alt rs193922474(C;C)
Reference rs193922474(G;G)
Significance Probable-Pathogenic
Disease Maturity-onset diabetes of the young
Variation info
Gene HNF4A
CLNDBN Maturity-onset diabetes of the young, type 1
Reversed 0
HGVS NC_000020.10:g.43043273G>C
CLNSRC ClinVar LabCorp
CLNACC RCV000030024.1,