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rs193922469

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922469(C;G)
Make rs193922469(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position44428368
GeneHNF4A
is asnp
is mentioned by
dbSNPrs193922469
ebirs193922469
HLIrs193922469
Exacrs193922469
Varsomers193922469
Maprs193922469
PheGenIrs193922469
hapmaprs193922469
1000 genomesrs193922469
hgdprs193922469
ensemblrs193922469
gopubmedrs193922469
geneviewrs193922469
scholarrs193922469
googlers193922469
pharmgkbrs193922469
gwascentralrs193922469
openSNPrs193922469
23andMers193922469
23andMe allrs193922469
SNP Nexus

SNPshotrs193922469
SNPdbers193922469
MSV3drs193922469
GWAS Ctlgrs193922469
Max Magnitude0
ClinVar
Risk rs193922469(A,G;A,G)
Alt rs193922469(A,G;A,G)
Reference rs193922469(C;C)
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.43057008C>G
CLNSRC ClinVar LabCorp
CLNACC RCV000030012.1,