Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs187438258
rs187438258
MYH2 ; MYHAS
0.010 GeneticVariation BEFREE Here, we describe the case of a motor developmental disorder associated with intellectual disability accompanied by <i>MYH2</i> mutations (c.2266G>A and c.4258C>T) in a female child in China. 30662633

2018