Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2284378
RALY
0.851 0.080 20 34000289 intron variant T/C;G snv 4
rs559848002
CDKN2A
0.925 0.120 9 21971147 missense variant T/C;G snv 4.7E-06 3
rs62068372
VPS9D1 ; ZNF276
0.925 0.080 16 89718699 intron variant T/C;G snv 2
rs6431588
ILKAP
0.925 0.040 2 238185147 intron variant T/C;G snv 0.86 0.85 2
rs7033503 1.000 0.040 9 21799599 upstream gene variant T/C;G snv 1
rs77064436
CTNNB1
1.000 0.040 3 41224577 missense variant T/C;G snv 1
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs758272654
GNAS
0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs121913513
KIT
0.776 0.120 4 54727495 missense variant T/C snv 10
rs4516035
VDR
0.776 0.360 12 47906043 non coding transcript exon variant T/C snv 0.31 10
rs2036534
HYKK
0.827 0.080 15 78534606 3 prime UTR variant T/C snv 0.26 8
rs10931936
CASP8
0.827 0.120 2 201279205 intron variant T/C snv 0.72 6
rs1512268
LOC107986930
0.851 0.160 8 23668950 intergenic variant T/C snv 0.50 6
rs587779826
ATM
0.851 0.360 11 108267344 splice donor variant T/C snv 4.0E-06 5
rs6914598
CDKAL1
0.851 0.080 6 21163688 intron variant T/C snv 0.38 4
rs1057519805
MAP2K1
1.000 0.040 15 66436839 missense variant T/C snv 3
rs1057519806
MAP2K2
0.882 0.200 19 4110583 missense variant T/C snv 3
rs1110400
MC1R
1.000 0.040 16 89919722 missense variant T/C snv 5.6E-03 6.6E-03 3
rs12512631 0.882 0.200 4 71735614 intergenic variant T/C snv 0.35 3
rs766310650
CDKN1A ; DINOL
1.000 0.040 6 36677906 5 prime UTR variant T/C snv 6.2E-05 2.1E-05 3
rs1057519702
KIT
1.000 0.040 4 54726020 missense variant T/C snv 2
rs1487774219
CDKN2B ; CDKN2B-AS1
1.000 0.040 9 22008910 missense variant T/C snv 8.1E-06 2
rs542002959
NLRP1
0.925 0.120 17 5558937 missense variant T/C snv 4.0E-06 1.4E-05 2
rs1051849
DUSP14
1.000 0.040 17 37513222 3 prime UTR variant T/C snv 9.9E-02 1
rs1057519812
PDGFRA
1.000 0.040 4 54277977 missense variant T/C snv 1