Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121909233
rs121909233
1.000 0.040 10 87864524 missense variant G/A snv
CUI: C0025202
Disease: melanoma
melanoma
0.800 0
dbSNP: rs121909234
rs121909234
1.000 0.040 10 87957867 missense variant G/A snv
CUI: C0025202
Disease: melanoma
melanoma
0.800 0
dbSNP: rs121913315
rs121913315
0.882 0.160 19 1220488 missense variant G/A;T snv
CUI: C0025202
Disease: melanoma
melanoma
0.800 1.000 0 1999 1999
dbSNP: rs121913351
rs121913351
0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06
CUI: C0025202
Disease: melanoma
melanoma
0.800 1.000 0 2013 2014
dbSNP: rs137853080
rs137853080
1.000 0.040 19 1207058 missense variant T/G snv
CUI: C0025202
Disease: melanoma
melanoma
0.800 0
dbSNP: rs137853081
rs137853081
1.000 0.040 19 1219352 missense variant G/C;T snv
CUI: C0025202
Disease: melanoma
melanoma
0.800 0
dbSNP: rs121913233
rs121913233
0.627 0.520 11 533874 missense variant T/A;C;G snv
CUI: C0025202
Disease: melanoma
melanoma
0.720 1.000 0 2016 2018
dbSNP: rs1064794292
rs1064794292
0.882 0.200 9 21974760 missense variant C/T snv
CUI: C0025202
Disease: melanoma
melanoma
0.710 1.000 0 2009 2009
dbSNP: rs397514606
rs397514606
0.763 0.320 1 243695714 missense variant C/T snv
CUI: C0025202
Disease: melanoma
melanoma
0.710 1.000 0 2008 2008
dbSNP: rs200476704
rs200476704
1.000 0.040 17 7930659 stop gained G/A;C snv 2.4E-05
CUI: C0025202
Disease: melanoma
melanoma
0.700 0
dbSNP: rs36204594
rs36204594
1.000 0.040 9 21971180 missense variant G/A;T snv
CUI: C0025202
Disease: melanoma
melanoma
0.700 0
dbSNP: rs80359204
rs80359204
1.000 0.040 13 32394741 missense variant A/G snv
CUI: C0025202
Disease: melanoma
melanoma
0.700 0