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: rs4785751
rs4785751
1.000 0.040 16 89963009 intron variant G/A snv 0.37
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2011 2011
dbSNP: rs7195043
rs7195043
1.000 0.040 16 89954453 intron variant C/T snv 0.58
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2011 2011
dbSNP: rs8051733
rs8051733
1.000 0.040 16 89957798 intron variant A/G snv 0.30
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2011 2011
dbSNP: rs1035142
rs1035142
0.807 0.200 2 201288355 3 prime UTR variant T/C;G snv 0.54
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2011 2011
dbSNP: rs13016963
rs13016963
0.851 0.080 2 201298088 intron variant A/G snv 0.59
CUI: C0025202
Disease: melanoma
melanoma
0.800 1.000 1 2011 2017
dbSNP: rs700635
rs700635
0.925 0.040 2 201288502 3 prime UTR variant C/A snv 0.72
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2011 2011
dbSNP: rs16953002
rs16953002
FTO
0.882 0.080 16 54080912 intron variant G/A snv 0.19
CUI: C0025202
Disease: melanoma
melanoma
0.800 1.000 1 2013 2017
dbSNP: rs1129038
rs1129038
0.851 0.120 15 28111713 3 prime UTR variant C/T snv 0.49 0.50
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2011 2011
dbSNP: rs12913832
rs12913832
0.763 0.200 15 28120472 intron variant A/G snv 0.50
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2011 2011
dbSNP: rs12380505
rs12380505
1.000 0.040 9 21695894 non coding transcript exon variant A/G snv 0.62
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
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: 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: 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: 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: 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: 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: 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