Source: GWASCAT

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: rs401681
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48
CUI: C0025202
Disease: melanoma
melanoma 		0.860 1.000 1 2010 2015
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 2 2011 2019
dbSNP: rs3219090
rs3219090
PARP1
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: rs7023329
rs7023329
MTAP
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: 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 2 2011 2017
dbSNP: rs910873
rs910873
PIGU
0.882 0.160 20 34583968 intron variant G/A;C snv
CUI: C0025202
Disease: melanoma
melanoma 		0.810 0.667 2 2008 2017
dbSNP: rs17119461
rs17119461
LINC02627
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: rs4698934
rs4698934
TET2 ; TET2-AS1
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: rs258322
rs258322
CDK10
0.925 0.120 16 89689495 intron variant A/G;T snv
CUI: C0025202
Disease: melanoma
melanoma 		0.800 1.000 4 2009 2017
dbSNP: rs1393350
rs1393350
TYR ; LOC107984363
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: rs13016963
rs13016963
FLACC1
0.851 0.080 2 201298088 intron variant A/G snv 0.59
CUI: C0025202
Disease: melanoma
melanoma 		0.800 1.000 2 2011 2017
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 2 2013 2017
dbSNP: rs2284063
rs2284063
PLA2G6
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 2 2009 2017
dbSNP: rs4785763
rs4785763
AFG3L1P
0.925 0.120 16 90000528 non coding transcript exon variant A/C;T snv
CUI: C0025202
Disease: melanoma
melanoma 		0.800 1.000 2 2009 2017
dbSNP: rs7412746
rs7412746
CTXND2
1.000 0.040 1 150887995 intron variant C/T snv 0.41
CUI: C0025202
Disease: melanoma
melanoma 		0.800 1.000 2 2011 2017
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
dbSNP: rs1805007
rs1805007
MC1R
0.695 0.280 16 89919709 missense variant C/A;G;T snv 4.4E-02
CUI: C0025202
Disease: melanoma
melanoma 		0.800 0.938 1 2001 2019
dbSNP: rs1885120
rs1885120
MYH7B ; MIR499A ; LOC107985393
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: rs35390
rs35390
SLC45A2
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: rs16891982
rs16891982
SLC45A2
0.776 0.200 5 33951588 missense variant C/A;G snv 0.65
CUI: C0025202
Disease: melanoma
melanoma 		0.750 0.833 1 2008 2017
dbSNP: rs187843643
rs187843643
LINC02218
1.000 0.040 5 17453974 intron variant C/T snv 3.9E-03
CUI: C0025202
Disease: melanoma
melanoma 		0.710 1.000 1 2017 2017
dbSNP: rs10739221
rs10739221
LINC01505
0.851 0.080 9 106298549 intron variant T/C;G snv
CUI: C0025202
Disease: melanoma
melanoma 		0.700 1.000 1 2017 2017
dbSNP: rs139996880
rs139996880
TERT
0.882 0.120 5 1284538 intron variant G/A snv 0.12
CUI: C0025202
Disease: melanoma
melanoma 		0.700 1.000 1 2017 2017
dbSNP: rs1636744
rs1636744
AHR
0.851 0.080 7 16944656 intron variant C/T snv 0.31
CUI: C0025202
Disease: melanoma
melanoma 		0.700 1.000 1 2017 2017
dbSNP: rs1847134
rs1847134
TYR ; LOC107984363
0.925 0.080 11 89272085 intron variant A/C snv 0.26
CUI: C0025202
Disease: melanoma
melanoma 		0.700 1.000 1 2014 2014