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

dbSNP: rs188675529
rs188675529
THAP11 ; CENPT
G 0.700 GeneticVariation CLINVAR

dbSNP: rs397515485
rs397515485
HCFC1
A 0.700 CausalMutation CLINVAR

dbSNP: rs397515486
rs397515486
HCFC1
A 0.700 CausalMutation CLINVAR

dbSNP: rs397515487
rs397515487
HCFC1
T 0.700 CausalMutation CLINVAR

dbSNP: rs398122908
rs398122908
HCFC1 ; TMEM187
G 0.700 CausalMutation CLINVAR

dbSNP: rs869312686
rs869312686
HCFC1
C 0.700 CausalMutation CLINVAR