Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs148149124
TUBGCP4
15 43382233 intron variant TAAAAGAAAAA/-;TAAAAGAAAAATAAAAGAAAAA delins 2
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 7
rs661171
ZC3H12C ; RDX
11 110145794 intron variant T/G snv 0.69 5
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 4
rs4495740
DOCK7
1 62658794 intron variant T/G snv 0.34 4
rs4917014 0.807 0.360 7 50266267 upstream gene variant T/G snv 0.26 4
rs5942937 X 110473179 intron variant T/G snv 0.47 4
rs12145743
RRNAD1
1 156730859 intron variant T/G snv 0.24 3
rs4082919
PGS1
17 78381401 intron variant T/G snv 0.55 3
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 3
rs6754295 1.000 0.040 2 20983311 regulatory region variant T/G snv 0.27 3
rs10426401
LOC107985305 ; PVR
1.000 0.080 19 44644419 intron variant T/G snv 0.32 2
rs2954026 8 125472284 intron variant T/G snv 0.76 2
rs3786247
LIPG
18 49592553 3 prime UTR variant T/G snv 0.13 2
rs4846923
GALNT2
1 230171476 intron variant T/G snv 0.72 2
rs545804325
MYO5B
18 49940996 intron variant T/G snv 1.4E-03 2
rs76376137 6 34205553 regulatory region variant T/G snv 3.9E-02 2
rs9638182 7 73584775 intergenic variant T/G snv 0.16 2
rs9923854
CETP
16 56983090 intron variant T/G snv 0.10 2
rs9939224
CETP
1.000 0.040 16 56968820 intron variant T/G snv 0.75 2
rs12708980
CETP
16 56978467 intron variant T/G snv 0.36 1
rs181360
UBE2L3
22 21574627 intron variant T/G snv 0.21 1
rs2472509
ABCA1
9 104921949 intron variant T/G snv 0.29 1
rs3211938
CD36
0.882 0.200 7 80671133 stop gained T/G snv 6.2E-03 2.6E-02 1
rs4148005
ABCA8
17 68886325 intron variant T/G snv 0.39 1