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: rs258322
rs258322
0.925 0.120 16 89689495 intron variant A/G;T snv
CUI: C0025202
Disease: melanoma
melanoma
0.800 1.000 5 2009 2017
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: 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: 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: 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: rs4785763
rs4785763
0.925 0.120 16 90000528 non coding transcript exon variant A/C;T snv
CUI: C0025202
Disease: melanoma
melanoma
0.800 1.000 1 2009 2017
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: rs7033503
rs7033503
1.000 0.040 9 21799599 upstream gene variant T/C;G 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: 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: 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: 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: rs1801516
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11
CUI: C0025202
Disease: melanoma
melanoma
0.810 1.000 1 2011 2017
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: 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: 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: 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: 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: 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: 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: 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: rs1341866
rs1341866
1.000 0.040 9 21771242 regulatory region variant T/C snv 0.34
CUI: C0025202
Disease: melanoma
melanoma
0.700 1.000 1 2012 2012
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: rs13097028
rs13097028
1.000 0.040 3 169747154 regulatory region variant C/T snv 0.38
CUI: C0025202
Disease: melanoma
melanoma
0.800 1.000 1 2014 2014