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: 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: rs291671
rs291671
1.000 0.040 20 33363039 intron variant G/A snv 0.92
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2008 2008
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: rs721970
rs721970
1.000 0.040 20 33315727 upstream gene variant A/G snv 0.96
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2008 2008
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: rs17305657
rs17305657
1.000 0.040 20 33218782 intron variant T/C snv 5.2E-02
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 2 2008 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: rs10852628
rs10852628
1.000 0.040 16 90013519 intron variant C/A;T snv
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2011 2011
dbSNP: rs10931936
rs10931936
0.827 0.120 2 201279205 intron variant T/C snv 0.72
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2011 2011
dbSNP: rs11076650
rs11076650
1.000 0.040 16 90001533 non coding transcript exon variant G/A snv 0.49
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2011 2011
dbSNP: rs11263498
rs11263498
1.000 0.040 11 69567999 TF binding site variant T/C snv 0.51
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2011 2011
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: rs11648898
rs11648898
1.000 0.040 16 89979578 non coding transcript exon variant A/G snv 0.17
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: 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: rs1485993
rs1485993
1.000 0.040 11 69547646 intergenic variant A/G snv 0.49
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2011 2011
dbSNP: rs228437
rs228437
1.000 0.040 6 134577318 intron variant C/A;G;T snv
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2011 2011
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: 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: rs4408545
rs4408545
1.000 0.040 16 89977620 non coding transcript exon variant C/G;T snv 0.40
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2011 2011
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: rs4785752
rs4785752
1.000 0.040 16 89968733 upstream gene variant A/G snv 0.42
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2011 2011
dbSNP: rs4785759
rs4785759
1.000 0.040 16 89984472 intron variant A/C;G snv
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2011 2011
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: 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