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: 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: rs7195043
rs7195043
DEF8
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: rs7848524
rs7848524
LOC107987026
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: rs8051733
rs8051733
DEF8
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: rs4238833
rs4238833
AFG3L1P
1.000 0.040 16 89984281 intron variant G/T snv 0.60
CUI: C0025202
Disease: melanoma
melanoma 		0.700 1.000 2 2011 2012
dbSNP: rs10757257
rs10757257
MTAP
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: rs132985
rs132985
PLA2G6
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: 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: rs2218220
rs2218220
LOC107987026
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: rs2353033
rs2353033
ANKRD11 ; LOC100287036
1.000 0.040 16 89319153 intron variant C/T snv 0.51
CUI: C0025202
Disease: melanoma
melanoma 		0.700 1.000 1 2012 2012
dbSNP: rs4636294
rs4636294
LOC107987026
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: rs7188458
rs7188458
SPATA33
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: rs738322
rs738322
PLA2G6
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: rs8059973
rs8059973
DBNDD1
1.000 0.040 16 90013126 intron variant A/G snv 0.78
CUI: C0025202
Disease: melanoma
melanoma 		0.700 1.000 1 2012 2012
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: rs4911414
rs4911414 		0.882 0.120 20 34141638 regulatory region variant T/G snv 0.73
CUI: C0025202
Disease: melanoma
melanoma 		0.710 1.000 1 2011 2013
dbSNP: rs1126809
rs1126809
TYR ; LOC107984363
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: 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: 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: rs4911442
rs4911442
NCOA6
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: rs1335510
rs1335510
LOC107987026
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: 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: rs258322
rs258322
CDK10
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: 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