Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs760077
MTX1 ; THBS3
0.925 0.120 1 155208991 missense variant T/A snv 0.36 7
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 6
rs1175550
SMIM1
1 3774964 intron variant A/G snv 0.31 5
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76 5
rs1569419
PRDM16
1 3080038 intron variant T/C snv 0.73 5
rs11211480
TAL1
1 47227548 non coding transcript exon variant A/G snv 0.42 3
rs12133576
DR1
1.000 0.040 1 93350843 intron variant A/G snv 0.51 3
rs2047007
MFSD2A
1 39962303 intron variant C/T snv 0.17 3
rs366684
PROX1
1 214013919 intron variant G/A;C snv 3
rs3813803
SMPDL3B
0.925 0.080 1 27955781 missense variant T/C snv 0.25 0.23 3
rs533281866
EGLN1
1 231422308 intron variant G/A;C snv 3
rs7529925
LINC01221
1 199038079 intron variant C/T snv 0.77 3
rs10494964
LOC105372912
1 213793544 intron variant T/C snv 0.45 2
rs10910476 1 234599210 regulatory region variant C/A;T snv 2
rs12734374
ASH1L
1.000 0.080 1 155419060 intron variant A/T snv 3.4E-02 2
rs148046772
CCT3
1 156314104 intron variant A/C;T snv 2
rs2072671
CDA
0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25 2
rs2274465
KDM4A
1 43655886 intron variant C/G snv 0.27 2
rs4846204
KIF1B
1 10248900 intron variant C/T snv 9.3E-02 2
rs646179
USP1
1 62437203 5 prime UTR variant A/G;T snv 2
rs72654647 1 24695823 TF binding site variant G/A snv 0.25 2
rs7520050
MAST2
1 45966433 intron variant A/C;G snv 2
rs78024727 1 198580649 intergenic variant G/A snv 3.5E-02 2