Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1034941983
rs1034941983
ADAM7 ; LOC101929294 ; LOC101929315
0.700 GeneticVariation UNIPROT

dbSNP: rs1169229302
rs1169229302
ADAM33
0.700 GeneticVariation UNIPROT

dbSNP: rs137990671
rs137990671
ADAM7 ; LOC101929294
0.700 GeneticVariation UNIPROT

dbSNP: rs140083180
rs140083180
ADAM29
0.700 GeneticVariation UNIPROT

dbSNP: rs150047888
rs150047888
ADAM29
0.700 GeneticVariation UNIPROT

dbSNP: rs150319320
rs150319320
ADAM7 ; LOC101929294
0.700 GeneticVariation UNIPROT

dbSNP: rs151030407
rs151030407
ADAM12
0.700 GeneticVariation UNIPROT

dbSNP: rs267600087
rs267600087
ADAM29
0.700 GeneticVariation UNIPROT

dbSNP: rs267600089
rs267600089
ADAM29
0.700 GeneticVariation UNIPROT

dbSNP: rs267600090
rs267600090
ADAM29
0.700 GeneticVariation UNIPROT

dbSNP: rs267600091
rs267600091
ADAM29
0.700 GeneticVariation UNIPROT

dbSNP: rs267600093
rs267600093
ADAM29
0.700 GeneticVariation UNIPROT

dbSNP: rs267601860
rs267601860
ADAM28 ; LOC101929294
0.700 GeneticVariation UNIPROT

dbSNP: rs267601862
rs267601862
ADAM28 ; LOC101929294
0.700 GeneticVariation UNIPROT

dbSNP: rs267601864
rs267601864
ADAM28 ; LOC101929294
0.700 GeneticVariation UNIPROT

dbSNP: rs267601866
rs267601866
ADAM7 ; LOC101929294
0.700 GeneticVariation UNIPROT

dbSNP: rs267601867
rs267601867
ADAM7 ; LOC101929294
0.700 GeneticVariation UNIPROT

dbSNP: rs267601868
rs267601868
ADAM7 ; LOC101929294
0.700 GeneticVariation UNIPROT

dbSNP: rs267601916
rs267601916
ADAM18
0.700 GeneticVariation UNIPROT

dbSNP: rs267601918
rs267601918
ADAM18
0.700 GeneticVariation UNIPROT

dbSNP: rs267604273
rs267604273
ADAM10
0.700 GeneticVariation UNIPROT

dbSNP: rs866380131
rs866380131
ADAM29
0.700 GeneticVariation UNIPROT

dbSNP: rs867202281
rs867202281
ADAM7 ; LOC101929294 ; LOC101929315
0.700 GeneticVariation UNIPROT

dbSNP: rs899870236
rs899870236
ADAM29
0.700 GeneticVariation UNIPROT

dbSNP: rs113488022
rs113488022
BRAF
0.040 GeneticVariation BEFREE Clinical and prognostic significance of BRAF V600E mutation in non-metastatic cutaneous melanoma patients. 31058533

2019