Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs999885
AP4M1 ; MCM7
0.925 0.120 7 100103553 intron variant G/A snv 0.56 0.46 3
rs13199764 6 100296258 regulatory region variant T/C snv 0.17 1
rs13196561 6 100312294 intergenic variant C/A snv 0.15 1
rs12894936
WDR25
14 100380654 intron variant T/C snv 0.55 1
rs10144321
WDR25
14 100416068 intron variant A/G snv 0.24 1
rs291269
PTPRD
9 10043773 intron variant A/G snv 0.39 1
rs78352137
WDR25
14 100454079 intron variant T/C snv 7.7E-02 2
rs12206564
ASCC3
6 100539133 intron variant T/C snv 0.49 1
rs6575793
BEGAIN
14 100565880 intron variant T/C snv 0.55 1
rs10119582
PTPRD
9 10060803 intron variant C/T snv 7.7E-02 1
rs239198
ASCC3
6 100686201 intron variant C/T snv 0.47 1
rs7141210 14 100716133 regulatory region variant T/C snv 0.55 2
rs1555406
DLK1
14 100737898 3 prime UTR variant C/T snv 0.12 1
rs10786610 10 100880906 TF binding site variant G/C;T snv 1
rs6575806
RTL1
14 100886874 intron variant C/A snv 0.72 1
rs7161194
MIR541
14 101062668 upstream gene variant A/G;T snv 2
rs10895140
TRPC6
11 101565990 intron variant A/G snv 0.62 1
rs10895141
TRPC6
11 101566010 intron variant A/C;T snv 0.62 1
rs4133019 1 102042537 intergenic variant A/C;G;T snv 1
rs11578152 1 102111465 intergenic variant A/G;T snv 1
rs1322148
PTPRD
9 10251492 intron variant A/T snv 0.57 1
rs56277911 2 10257226 intergenic variant C/T snv 7.8E-02 1
rs7865468
PTPRD
9 10274080 intron variant G/A;C snv 1
rs10820310 9 102923803 downstream gene variant A/G snv 0.28 1
rs7662107
LINC02428
4 103337239 intron variant C/T snv 0.26 1