Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913388
CDKN2A
0.925 0.040 9 21971121 stop gained G/A;C snv 4.4E-06 2
rs121913523
KIT
1.000 0.040 4 54728092 missense variant T/A;C snv 2
rs137853080
STK11
1.000 0.040 19 1207058 missense variant T/G snv 2
rs137853081
STK11
1.000 0.040 19 1219352 missense variant G/C;T snv 2
rs138106763
SLC12A9
1.000 0.040 7 100857102 missense variant A/G snv 7.2E-05 1.2E-04 2
rs1449409868
SSTR4
0.925 0.040 20 23035958 missense variant C/A;T snv 4.1E-06; 4.1E-06 2
rs1487774219
CDKN2B ; CDKN2B-AS1
1.000 0.040 9 22008910 missense variant T/C snv 8.1E-06 2
rs1554653960
CDKN2A
0.925 0.040 9 21971007 missense variant C/T snv 2
rs1885120
LOC107985393 ; MIR499A ; MYH7B
1.000 0.040 20 34989186 intron variant C/G snv 0.96 2
rs200375589
KIT
1.000 0.040 4 54727442 missense variant G/A;C;T snv 6.0E-05 2
rs2074560
MX2
0.925 0.040 21 41380411 intron variant A/G snv 0.43 2
rs215605
PDE1C
1.000 0.040 7 32297353 intron variant G/T snv 0.54 2
rs2353033
LOC100287036 ; ANKRD11
1.000 0.040 16 89319153 intron variant C/T snv 0.51 2
rs291671
CDK5RAP1
1.000 0.040 20 33363039 intron variant G/A snv 0.92 2
rs36204594
CDKN2A
1.000 0.040 9 21971180 missense variant G/A;T snv 2
rs397514644
AKT1
0.925 0.040 14 104780190 missense variant G/A snv 7.0E-06 2
rs4238833
AFG3L1P
1.000 0.040 16 89984281 intron variant G/T snv 0.60 2
rs4408545
AFG3L1P
1.000 0.040 16 89977620 non coding transcript exon variant C/G;T snv 0.40 2
rs4608623
PLA2G6 ; MAFF
0.925 0.040 22 38201371 non coding transcript exon variant G/T snv 0.52 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
rs4911442
NCOA6
1.000 0.040 20 34767243 intron variant G/A snv 0.93 2
rs62389423 1.000 0.040 6 421281 intergenic variant G/A;T snv 8.5E-02 2
rs6431588
ILKAP
0.925 0.040 2 238185147 intron variant T/C;G snv 0.86 0.85 2
rs7023954
MTAP
0.925 0.040 9 21816759 missense variant G/A snv 0.40 0.42 2