Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606771
rs267606771
DMD
0.710 GeneticVariation BEFREE A nonsense mutation (E1211X) due to a G to T transversion at the 28th nucleotide of exon 27 (G3839T) was identified in the dystrophin gene of a Japanese Becker muscular dystrophy case. 9410897

1997
dbSNP: rs267606771
rs267606771
DMD
A 0.710 CausalMutation CLINVAR