Disease: Cutaneous Melanoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12696304 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 10
rs380286
CLPTM1L
0.776 0.200 5 1320132 intron variant G/A snv 0.47 8
rs35158985
CDH1
0.882 0.080 16 68762843 intron variant A/G snv 0.38 6
rs4778138
OCA2
0.851 0.080 15 28090674 intron variant A/G;T snv 6
rs10739221
LINC01505
0.851 0.080 9 106298549 intron variant T/C;G snv 5
rs132985
PLA2G6
0.827 0.120 22 38167464 intron variant C/T snv 0.51 5
rs251464
PPARGC1B
0.851 0.080 5 149816671 intron variant G/C snv 0.36 5
rs10816595 0.851 0.080 9 107947454 regulatory region variant A/G snv 0.33 4
rs10830253
TYR
0.851 0.080 11 89294875 intron variant T/G snv 0.29 4
rs1636744
AHR
0.851 0.080 7 16944656 intron variant C/T snv 0.31 4
rs2995264
STN1
0.851 0.080 10 103909085 intron variant G/A snv 0.88 4
rs34466956
NFIC
0.882 0.080 19 3353624 intron variant C/T snv 0.49 4
rs498136 0.851 0.080 11 69552350 intergenic variant A/C snv 0.68 4
rs56238684
PIGU
0.882 0.080 20 34648892 intron variant G/C snv 4.2E-02 4
rs6750047
RMDN2
0.851 0.080 2 38049406 intron variant A/G snv 0.61 4
rs6914598
CDKAL1
0.851 0.080 6 21163688 intron variant T/C snv 0.38 4
rs75570604
FANCA
0.851 0.080 16 89780269 intron variant G/C snv 4.7E-02 4
rs869329
MTAP
0.851 0.080 9 21804694 intron variant A/G;T snv 4
rs1148732
MIR614 ; GPRC5A
0.882 0.080 12 12915357 3 prime UTR variant G/A;C snv 3
rs11532907
MTAP
0.882 0.080 9 21844773 intron variant A/G;T snv 3
rs117648907
FMN1
0.882 0.080 15 32985509 intron variant C/T snv 1.4E-02 3
rs12596638
FTO
0.882 0.080 16 54081917 intron variant G/A snv 0.18 3
rs1484375
LINC01505
0.882 0.080 9 106305280 intron variant A/G;T snv 3
rs1640875
GPRC5A
0.882 0.080 12 12916590 3 prime UTR variant A/T snv 0.49 3
rs184628474
TTC7B
0.882 0.080 14 90719521 intron variant G/A snv 2.9E-02 3