Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63750710
rs63750710
MLH1
0.710 GeneticVariation BEFREE Thus, the H329P mutation present in the germline can be considered as having an aetiological role in this HNPCC family. 9272156

1997
dbSNP: rs63750710
rs63750710
MLH1
C 0.710 CausalMutation CLINVAR