Gene: CHRND ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909506
rs121909506
CHRND
0.800 GeneticVariation UNIPROT Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders. 18252226

2008
dbSNP: rs121909506
rs121909506
CHRND
C 0.800 CausalMutation CLINVAR

dbSNP: rs121909505
rs121909505
CHRND
A 0.700 CausalMutation CLINVAR Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders. 18252226

2008
dbSNP: rs1060499782
rs1060499782
CHRND
G 0.700 GeneticVariation CLINVAR

dbSNP: rs121909507
rs121909507
CHRND
T 0.700 CausalMutation CLINVAR