Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17561351
NECTIN2
19 44869072 intron variant A/G snv 5.2E-02 1
rs185387034
PDYN-AS1
20 1970274 intron variant A/G snv 4.6E-03 1
rs2075371
SLC35B4
7 134299375 3 prime UTR variant A/G snv 0.49 1
rs2303149
TPM4
19 16086611 intron variant A/G snv 0.52 1
rs35304300 6 139536204 intron variant A/G snv 0.15 1
rs4764487
LOC105369625 ; CD9
12 6223672 intron variant A/G snv 0.72 1
rs4777161
DRAIC
15 69569200 intron variant A/G snv 0.81 1
rs56133113
ARAP1 ; STARD10
11 72790175 intron variant A/G snv 9.3E-02 1
rs6099612 20 57411745 downstream gene variant A/G snv 0.16 1
rs647316
EHD3
2 31241963 intron variant A/G snv 0.80 1
rs6759839 2 16439535 intergenic variant A/G snv 0.56 1
rs7075195
JMJD1C
10 63290899 intron variant A/G snv 0.38 1
rs73076965
LOC105372499 ; SIRPD
20 1535534 intron variant A/G snv 0.16 1
rs7596219 2 66415818 intergenic variant A/G snv 0.14 1
rs77327054
DCAF5
14 69129366 intron variant A/G snv 4.2E-02 1
rs7743045
SELENOKP3
6 118781108 intron variant A/G snv 0.65 1
rs896322
LOC101929459 ; TMCC2
1 205240617 intron variant A/G snv 0.92 1
rs2038480
DNM3
1 171970501 intron variant A/G;T snv 2
rs11920280
KALRN
3 124618265 intron variant A/G;T snv 1
rs12271225
TRIM5
11 5669314 intron variant A/G;T snv 0.17 1
rs4674740
KCNE4 ; LOC105373905
2 223107409 intron variant A/G;T snv 1
rs6681480
DNM3
1 171925452 intron variant A/G;T snv 1
rs6992820 8 55851897 TF binding site variant A/G;T snv 1
rs7208363
TAOK1
17 29406390 intron variant A/G;T snv 1
rs7213208
TAOK1
17 29405851 intron variant A/G;T snv 1