Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587779766
rs587779766
AHDC1
CUI: C1843367
Disease: Poor school performance
Poor school performance 		C 0.700 CausalMutation CLINVAR De novo truncating mutations in AHDC1 in individuals with syndromic expressive language delay, hypotonia, and sleep apnea. 24791903

2014
dbSNP: rs587779767
rs587779767
AHDC1
CUI: C1843367
Disease: Poor school performance
Poor school performance 		A 0.700 CausalMutation CLINVAR De novo truncating mutations in AHDC1 in individuals with syndromic expressive language delay, hypotonia, and sleep apnea. 24791903

2014
dbSNP: rs587779768
rs587779768
AHDC1
CUI: C1843367
Disease: Poor school performance
Poor school performance 		A 0.700 CausalMutation CLINVAR De novo truncating mutations in AHDC1 in individuals with syndromic expressive language delay, hypotonia, and sleep apnea. 24791903

2014