Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63750899
rs63750899
MLH1
0.710 GeneticVariation BEFREE Here, we describe a mutation, MLH1 P648S, which was found in a typical HNPCC family, with one homozygous child displaying mild features of NF1 and no hematological cancers. 15139004

2004
dbSNP: rs63750899
rs63750899
MLH1
T 0.710 CausalMutation CLINVAR