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rs193922477

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922477(C;C)
Make rs193922477(C;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position44419818
GeneHNF4A
is asnp
is mentioned by
dbSNPrs193922477
ebirs193922477
HLIrs193922477
Exacrs193922477
Varsomers193922477
Maprs193922477
PheGenIrs193922477
hapmaprs193922477
1000 genomesrs193922477
hgdprs193922477
ensemblrs193922477
gopubmedrs193922477
geneviewrs193922477
scholarrs193922477
googlers193922477
pharmgkbrs193922477
gwascentralrs193922477
openSNPrs193922477
23andMers193922477
23andMe allrs193922477
SNP Nexus

SNPshotrs193922477
SNPdbers193922477
MSV3drs193922477
GWAS Ctlgrs193922477
Max Magnitude0
ClinVar
Risk rs193922477(C;C)
Alt rs193922477(C;C)
Reference rs193922477(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.43048458G>C
CLNSRC ClinVar LabCorp
CLNACC RCV000030030.1,