Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 7
rs10761731
JMJD1C
10 63267850 intron variant A/T snv 0.38 6
rs114694170
MEF2C ; MEF2C-AS1
1.000 0.040 5 88884379 non coding transcript exon variant T/C snv 3.6E-02 4
rs10761741
JMJD1C
1.000 0.040 10 63306426 intron variant G/T snv 0.38 3
rs2375980 9 2692622 intergenic variant C/G snv 0.51 2
rs6479877 10 63118358 intergenic variant C/A;G;T snv 2
rs6921438 0.776 0.360 6 43957870 intergenic variant G/A;C snv 2
rs7767396 6 43959313 intergenic variant A/G snv 0.48 2
rs12199215
LOC101929705
6 44059177 non coding transcript exon variant C/T snv 0.25 2
rs4782371
ZFPM1
1.000 0.040 16 88502423 intron variant T/A;G snv 2
rs10738760 0.807 0.320 9 2691186 regulatory region variant A/G snv 0.56 1
rs12214617 6 43972186 intergenic variant G/T snv 0.53 1
rs143479231 3 193393005 intergenic variant G/A snv 1.5E-02 1
rs1740073 1.000 0.040 6 43979661 regulatory region variant T/C snv 0.67 1
rs2375981 1.000 0.040 9 2692583 regulatory region variant C/G;T snv 1
rs34528081 6 43736680 intron variant -/T ins 0.49 1
rs4513773 6 43957789 intergenic variant A/G snv 0.44 1
rs7030781 9 2686273 intergenic variant A/G;T snv 1
rs7763358
CAPN11
6 44172132 intron variant C/T snv 7.8E-02 1
rs144085478
CDC5L
6 44432305 intron variant T/C snv 8.9E-03 1
rs186725382
EVC2
4 5634346 intron variant G/A snv 5.4E-04 1
rs10761750
JMJD1C
10 63368859 intron variant G/A snv 0.43 1
rs34524635
JMJD1C
10 63501417 intron variant T/- delins 0.43 1
rs9472155
LINC01512
6 43929990 intergenic variant C/T snv 0.28 1
rs144820908
LOC105375075
6 44545748 intergenic variant A/C snv 4.0E-03 1