Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057517688
rs1057517688
Entrez Id: 84879
Gene Symbol: MFSD2A
MFSD2A
CUI: C4225310
Disease:
MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE
T 0.800 CausalMutation CLINVAR
dbSNP: rs1057517688
rs1057517688
Entrez Id: 84879
Gene Symbol: MFSD2A
MFSD2A
CUI: C4225310
Disease:
MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE
0.800 GeneticVariation UNIPROT