Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1281877795
rs1281877795
Entrez Id: 4528
Gene Symbol: MTIF2
MTIF2
CUI: C0432072
Disease:
Dysmorphic features 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1281877795
rs1281877795
Entrez Id: 4528
Gene Symbol: MTIF2
MTIF2
CUI: C0000772
Disease:
Multiple congenital anomalies 		G 0.700 GeneticVariation CLINVAR