Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs318240758
rs318240758
HCFC1
0.800 GeneticVariation UNIPROT A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disability. 23000143

2012
dbSNP: rs318240758
rs318240758
HCFC1
T 0.800 CausalMutation CLINVAR