Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35883536
LINC01349
1 100640978 non coding transcript exon variant G/A snv 0.46 2
rs4807440
CNN2
19 1026478 upstream gene variant G/T snv 0.65 3
rs562752749
WBP1L
10 102805443 intron variant TT/-;T;TTT;TTTT;TTTTT;TTTTTTT;TTTTTTTTTTTT delins 2
rs12898000 14 103368791 upstream gene variant G/C;T snv 2
rs8022179 14 103380950 upstream gene variant T/A;C snv 2
rs7298732 12 10458392 upstream gene variant T/C snv 9.8E-02 2
rs199741557 4 104943373 intron variant TC/- delins 2.6E-02 2
rs605783
GCNT2
6 10526140 intron variant T/A snv 0.65 2
rs9480737 6 107121073 intergenic variant A/G snv 0.33 2
rs12312487
CMKLR1
12 108327859 intron variant G/A snv 0.31 2
rs150861794 13 108351457 intron variant C/T snv 1.7E-02 2
rs75900305
LOC105370356 ; MYO16
13 109159737 intron variant -/C delins 0.25 2
rs1887639
LOC105370359
13 109374581 intergenic variant T/C snv 0.42 2
rs17608459
LINC01768
1 109892706 upstream gene variant G/A snv 7.9E-02 2
rs333947
CSF1
1 109928142 intron variant G/A snv 0.13 7
rs58814158
COL4A1
13 110167908 intron variant T/G snv 0.12 2
rs2062225
ACOXL
2 110993295 intron variant A/C;T snv 2
rs150449635
ACOXL
2 110994574 intron variant T/C snv 1.5E-02 2
rs3789088
ACOXL ; MIR4435-2HG
2 111033227 intron variant G/C snv 0.14 2
rs3789087
ACOXL ; MIR4435-2HG
2 111034076 intron variant C/T snv 0.14 2
rs7578982
ACOXL ; MIR4435-2HG
2 111078961 intron variant T/C snv 0.27 2
rs10980797
LOC105376219
9 111150273 intron variant A/G;T snv 3
rs6734942
MIR4435-2HG ; BCL2L11
2 111153117 intron variant C/G;T snv 2
rs10980800
LOC105376219
9 111153625 intron variant T/C snv 0.21 2
rs12346772
LOC105376219
9 111158319 intron variant A/G snv 0.18 2