Source: GWASDB

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: rs1393350
rs1393350
0.851 0.160 11 89277878 intron variant G/A snv 0.17
CUI: C0025202
Disease: melanoma
melanoma
0.800 1.000 3 2009 2017
dbSNP: rs1126809
rs1126809
0.683 0.320 11 89284793 missense variant G/A snv 0.18 0.18
CUI: C0025202
Disease: melanoma
melanoma
0.730 1.000 1 2008 2014
dbSNP: rs4698934
rs4698934
1.000 0.040 4 105218230 intron variant T/C snv 0.12
CUI: C0025202
Disease: melanoma
melanoma
0.810 1.000 1 2014 2014
dbSNP: rs7188458
rs7188458
1.000 0.040 16 89660076 3 prime UTR variant G/A;T snv 0.45
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2012 2012
dbSNP: rs35390
rs35390
1.000 0.040 5 33955221 intron variant C/A snv 0.81
CUI: C0025202
Disease: melanoma
melanoma
0.800 1.000 1 2011 2011
dbSNP: rs132985
rs132985
0.827 0.120 22 38167464 intron variant C/T snv 0.51
CUI: C0025202
Disease: melanoma
melanoma
0.710 1.000 1 2009 2012
dbSNP: rs2284063
rs2284063
0.851 0.160 22 38148291 non coding transcript exon variant A/G snv 0.40
CUI: C0025202
Disease: melanoma
melanoma
0.800 1.000 1 2009 2017
dbSNP: rs738322
rs738322
0.925 0.040 22 38172999 intron variant A/G snv 0.52
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2012 2012
dbSNP: rs910873
rs910873
0.882 0.160 20 34583968 intron variant G/A;C snv
CUI: C0025202
Disease: melanoma
melanoma
0.810 0.667 1 2008 2017
dbSNP: rs6058339
rs6058339
1.000 0.040 20 35872557 intron variant C/T snv 0.94
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2008 2008
dbSNP: rs3219090
rs3219090
1.000 0.040 1 226376990 intron variant T/C snv 0.58
CUI: C0025202
Disease: melanoma
melanoma
0.820 1.000 1 2011 2013
dbSNP: rs1204552
rs1204552
1.000 0.040 20 36050981 non coding transcript exon variant T/A;C;G snv
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2008 2008
dbSNP: rs4911442
rs4911442
1.000 0.040 20 34767243 intron variant G/A snv 0.93
CUI: C0025202
Disease: melanoma
melanoma
0.720 1.000 1 2008 2014
dbSNP: rs7271289
rs7271289
1.000 0.040 20 34809500 5 prime UTR variant C/T snv 0.15
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2008 2008
dbSNP: rs1885120
rs1885120
1.000 0.040 20 34989186 intron variant C/G snv 0.96
CUI: C0025202
Disease: melanoma
melanoma
0.800 1.000 1 2008 2017
dbSNP: rs45430
rs45430
MX2
1.000 0.040 21 41374154 intron variant C/T snv 0.48
CUI: C0025202
Disease: melanoma
melanoma
0.820 1.000 1 2011 2019
dbSNP: rs7023329
rs7023329
0.790 0.160 9 21816529 intron variant A/G snv 0.50
CUI: C0025202
Disease: melanoma
melanoma
0.810 1.000 3 2009 2017
dbSNP: rs10757257
rs10757257
0.882 0.080 9 21806565 intron variant G/A snv 0.34
CUI: C0025202
Disease: melanoma
melanoma
0.710 1.000 1 2009 2012
dbSNP: rs1335510
rs1335510
1.000 0.040 9 21757804 intergenic variant T/G snv 0.32
CUI: C0025202
Disease: melanoma
melanoma
0.710 1.000 1 2012 2015
dbSNP: rs2218220
rs2218220
1.000 0.040 9 21756090 intergenic variant C/T snv 0.60
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2012 2012
dbSNP: rs2383202
rs2383202
1.000 0.040 9 21710216 regulatory region variant C/T snv 0.61
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2011 2011
dbSNP: rs4636294
rs4636294
0.925 0.040 9 21747804 intergenic variant A/G snv 0.61
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2012 2012
dbSNP: rs6475552
rs6475552
1.000 0.040 9 21701675 downstream gene variant G/A;T snv
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2011 2011
dbSNP: rs7848524
rs7848524
1.000 0.040 9 21701433 downstream gene variant T/A;C;G snv
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2011 2011
dbSNP: rs17119461
rs17119461
1.000 0.040 10 105756594 intergenic variant T/C snv 7.7E-02
CUI: C0025202
Disease: melanoma
melanoma
0.810 1.000 1 2012 2014