Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs62305038
DAPP1
4 99839008 intron variant C/T snv 0.33 2
rs10883353 10 99496351 intergenic variant G/A snv 0.82 2
rs2301889
ARPC1A
7 99333482 intron variant A/G snv 0.13 2
rs7182976
IGF1R
15 98753427 intron variant C/A;T snv 2
rs1573891 15 98643259 downstream gene variant G/C snv 0.32 3
rs12376113 9 97958017 regulatory region variant G/C snv 0.11 2
rs2449511
MTDH
8 97723714 intron variant A/G snv 9.2E-02 2
rs2468024
MTDH
8 97652425 intron variant G/A;C snv 3
rs1155998 8 97639920 upstream gene variant C/A snv 0.22 2
rs415895
SWAP70
11 9748015 missense variant C/G snv 0.62 0.61 6
rs3017756
CEP57
11 95804194 intron variant G/A snv 0.35 2
rs11021221 11 95575690 intron variant T/A;G snv 4
rs632087
LOC101929295
11 95152471 intron variant C/T snv 0.59 2
rs7078811
HELLS
10 94596424 intron variant C/T snv 0.45 2
rs9409793
LOC107987100
9 94508873 intron variant C/A;G snv 2
rs35219595
LOC107987100
9 94506901 intron variant G/- delins 0.69 2
rs67183237
TBC1D12
10 94486139 intron variant C/T snv 2
rs11187938
TBC1D12
10 94423594 intron variant T/C snv 0.51 2
rs10821339
LOC105376154 ; NUTM2F
9 94324185 intron variant G/A snv 0.28 2
rs113792729
LOC643339
12 93326892 intron variant A/G snv 0.33 2
rs739385 7 93053295 regulatory region variant G/A;C snv 4
rs2774952
DIPK1A
1 92889689 intron variant A/C snv 0.68 2
rs78084721 13 91366396 intergenic variant G/A snv 2.0E-02 2
rs10801851
HFM1
1 91281449 intron variant C/T snv 0.48 2
rs17515485
VPS33B-DT
15 91030274 intron variant T/G snv 6.4E-02 2