Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13001130
AFF3
2 100052237 intron variant G/A snv 0.15 1
rs78633727
AFF3
2 100052995 intron variant T/C snv 0.16 1
rs6750720
AFF3
2 100054283 intron variant C/G;T snv 1
rs6714788
AFF3
2 100069711 intron variant C/A;T snv 1
rs72774059
GRIN2A
16 10007295 intron variant C/A;T snv 1
rs11596211
CPN1
10 100080362 intron variant T/A snv 0.25 1
rs4851250
AFF3
2 100112831 intron variant T/C;G snv 1
rs2309752
AFF3
2 100145707 intron variant T/A;G snv 1
rs4851254
AFF3
2 100146475 intron variant C/G;T snv 1
rs1408579
ERLIN1
1.000 0.040 10 100152437 intron variant C/T snv 0.32 3
rs11123816
AFF3
2 100167191 intron variant G/A snv 0.20 1
rs7583067
AFF3
2 100180388 intron variant C/A;T snv 1
rs12712073
AFF3
2 100188666 intron variant T/C snv 0.33 1
rs6712515
AFF3
0.925 0.160 2 100190052 intron variant T/A;C snv 3
rs837705
GRIN2A
16 10019519 intron variant C/A snv 0.69 1
rs13018640 2 100205083 upstream gene variant T/C;G snv 1
rs9653442
LINC01104
1.000 0.120 2 100208905 intron variant C/T snv 0.46 2
rs10865035
LINC01104
1.000 0.080 2 100219272 intron variant A/G snv 0.42 1
rs13010010
LINC01104
2 100236272 intron variant C/T snv 0.27 1
rs2309812 2 100253240 downstream gene variant C/A;T snv 1
rs4331524 2 100259649 intergenic variant C/T snv 0.34 1
rs4438499 2 100260327 intergenic variant G/A snv 0.45 1
rs2067783 2 100260908 regulatory region variant T/C snv 0.39 1
rs61871342
BLOC1S2
1.000 0.040 10 100278884 intron variant G/A snv 0.36 2
rs7582180
LONRF2
2 100296001 intron variant A/G snv 0.72 1