Gene: AHDC1 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587779768
rs587779768
AHDC1
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: rs1135401761
rs1135401761
AHDC1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1165205177
rs1165205177
AHDC1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1165205177
rs1165205177
AHDC1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1553158393
rs1553158393
AHDC1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1553158517
rs1553158517
AHDC1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1553159383
rs1553159383
AHDC1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553159764
rs1553159764
AHDC1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1553159979
rs1553159979
AHDC1
G 0.700 CausalMutation CLINVAR

dbSNP: rs1557655967
rs1557655967
AHDC1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1557667078
rs1557667078
AHDC1
G 0.700 CausalMutation CLINVAR

dbSNP: rs587779766
rs587779766
AHDC1
C 0.700 CausalMutation CLINVAR

dbSNP: rs587779767
rs587779767
AHDC1
A 0.700 CausalMutation CLINVAR

dbSNP: rs886039900
rs886039900
AHDC1
A 0.700 CausalMutation CLINVAR