Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10460181
LOC107985305 ; IGSF23
19 44636865 intron variant A/G;T snv 0.26 2
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 6
rs10490626
LOC107985940
2 118078265 intergenic variant G/A snv 5.2E-02 2
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 3
rs1062062
TBC1D8 ; RPL31
2 101011463 missense variant C/T snv 9.8E-02 9.3E-02 1
rs1065853 19 44909976 non coding transcript exon variant G/A;C;T snv 4
rs10692845 2 21070463 regulatory region variant -/GA;GACTCAAAGTACACATTTCCTAGA delins 0.69 1
rs10738607
CDKN2B-AS1
0.925 0.080 9 22088095 intron variant A/G snv 0.42 3
rs10744826
UBE3B
12 109527707 intron variant C/G snv 0.57 3
rs1077514
ASAP3
1 23439740 intron variant C/T snv 0.75 1
rs1077834
LIPC ; ALDH1A2
15 58431280 intron variant T/C snv 0.34 4
rs1077835
ALDH1A2 ; LIPC
15 58431227 intron variant A/G snv 0.34 3
rs10808546 8 125483576 intron variant C/T snv 0.39 6
rs10832027
ARNTL
11 13335636 intron variant G/A snv 0.67 5
rs10832962
SPTY2D1 ; LOC105376578
11 18634724 non coding transcript exon variant C/T snv 0.55 1
rs10876041
DIP2B
12 50508099 intron variant T/C snv 0.58 4
rs10889333
DOCK7
1 62491359 intron variant G/A snv 0.33 1
rs10889348
DOCK7
1 62612551 intron variant A/T snv 0.32 3
rs10889353
DOCK7
1 62652525 intron variant A/C;T snv 4
rs10893499
ST3GAL4
11 126372084 intron variant G/A snv 0.16 2
rs10900522
NUCKS1
1 205714939 3 prime UTR variant T/C snv 0.21 4
rs10903129
MACO1
1 25442446 intron variant A/G snv 0.58 3
rs10904908
VIM-AS1
10 17218291 intron variant A/G snv 0.41 1
rs11024735
SPTY2D1
11 18617620 intron variant C/G;T snv 2
rs11048456
LOC105369705
1.000 0.080 12 26310149 intron variant C/T snv 0.62 6