Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10816595 0.851 0.080 9 107947454 regulatory region variant A/G snv 0.33 4
rs1232547491
RHCE
0.851 0.120 1 25385838 missense variant A/G snv 4
rs2284063
PLA2G6
0.851 0.160 22 38148291 non coding transcript exon variant A/G snv 0.40 4
rs6750047
RMDN2
0.851 0.080 2 38049406 intron variant A/G snv 0.61 4
rs794729219
BRAF
0.882 0.240 7 140753352 missense variant A/G snv 3
rs138106763
SLC12A9
1.000 0.040 7 100857102 missense variant A/G snv 7.2E-05 1.2E-04 2
rs2074560
MX2
0.925 0.040 21 41380411 intron variant A/G snv 0.43 2
rs4636294
LOC107987026
0.925 0.040 9 21747804 intergenic variant A/G snv 0.61 2
rs4785752 1.000 0.040 16 89968733 upstream gene variant A/G snv 0.42 2
rs738322
PLA2G6
0.925 0.040 22 38172999 intron variant A/G snv 0.52 2
rs7944031
TEAD1
0.925 0.080 11 12907573 intron variant A/G snv 0.21 2
rs869330
MTAP
0.925 0.080 9 21804618 intron variant A/G snv 0.62 2
rs947005337
POT1
0.925 0.120 7 124870933 missense variant A/G snv 1.6E-05 1.4E-05 2
rs1057519705
KIT
1.000 0.040 4 54727464 missense variant A/G snv 1
rs1060502550
KIT
1.000 0.040 4 54727488 missense variant A/G snv 1
rs11568953
EGF
1.000 0.040 4 109963240 synonymous variant A/G snv 9.7E-03 1.0E-02 1
rs11648898
AFG3L1P
1.000 0.040 16 89979578 non coding transcript exon variant A/G snv 0.17 1
rs1176796243
MITF
1.000 0.040 3 69941240 missense variant A/G snv 1
rs1194330242
MGRN1
1.000 0.040 16 4681743 missense variant A/G snv 1.4E-05 1
rs121913225
BRAF
1.000 0.040 7 140753351 missense variant A/G snv 1
rs12380505
KHSRPP1
1.000 0.040 9 21695894 non coding transcript exon variant A/G snv 0.62 1
rs1485993 1.000 0.040 11 69547646 intergenic variant A/G snv 0.49 1
rs2127675 1.000 0.040 6 32883073 upstream gene variant A/G snv 0.36 1
rs2301641
ABCB5
1.000 0.040 7 20658647 missense variant A/G snv 0.33 0.40 1
rs2981096
TERF1
1.000 0.040 8 73027927 intron variant A/G snv 3.1E-02 1