Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9650622 8 9946782 intergenic variant G/T snv 0.40 2
rs13271489 8 9946202 intergenic variant T/C snv 0.38 2
rs187821766
STK3
8 98729050 intron variant C/T snv 3.5E-03 3
rs186208701
STK3
8 98567888 intron variant T/C snv 3.3E-03 3
rs4841235 8 9825848 intergenic variant A/G snv 0.56 2
rs55868514 8 9822890 intergenic variant T/C snv 0.57 2
rs187222839 11 98073424 intergenic variant T/C snv 1.6E-03 1
rs9286060 8 9795635 intergenic variant A/C;T snv 2
rs11599481
CRTAC1
10 97880706 intron variant C/T snv 0.19 2
rs4851462
ZAP70
2 97740700 downstream gene variant T/C snv 0.29 1
rs4910498
SWAP70
11 9743956 intron variant A/T snv 0.61 4
rs2649044
SWAP70
11 9742422 intron variant C/T snv 0.55 4
rs360153
SWAP70
11 9740727 non coding transcript exon variant T/C snv 0.57 1
rs55684003
MBNL2
13 97336435 intron variant A/G snv 0.22 1
rs360158
SWAP70
11 9732054 intron variant G/A snv 0.66 2
rs7902871
SLIT1
10 97049946 intron variant A/G snv 0.21 2
rs1947228 7 96832337 regulatory region variant T/A;C snv 1
rs7599598
FER1L5
2 96686103 missense variant A/G;T snv 0.41 2
rs35410524
UFL1-AS1
6 96437529 intron variant C/T snv 0.15 2
rs1081707 2 96381261 downstream gene variant G/A snv 0.24 1
rs7134060
CDK17
12 96323317 intron variant G/A snv 0.36 1
rs772178
SNRNP200
2 96297946 intron variant A/C;G snv 1
rs4984497
LOC112268156 ; LOC105369212
15 96092670 intron variant T/C snv 0.76 1
rs4984496
LOC112268156 ; LOC105369212
15 96092669 intron variant T/G snv 0.76 1
rs2579519
FAHD2CP
2 96009418 upstream gene variant T/C snv 0.37 1