Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786204798
rs786204798
ADCY6 ; TEX49
A 0.800 CausalMutation CLINVAR

dbSNP: rs786204798
rs786204798
ADCY6 ; TEX49
0.800 GeneticVariation UNIPROT

dbSNP: rs879253864
rs879253864
ADCY6 ; MIR4701
C 0.700 GeneticVariation CLINVAR Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy. 26257172

2015