Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72996113 11 100582315 intergenic variant C/T snv 7.8E-02 1
rs564636753
TFR2
7 100639580 intron variant A/-;AA;AAA;AAAA delins 1
rs4434553
TFR2
1.000 0.040 7 100642568 intron variant A/G snv 0.40 1
rs667575
ARHGAP42
11 100767524 intron variant G/A snv 0.76 1
rs77822621
FGFRL1
4 1014424 intron variant C/G;T snv 1
rs139141690
CUX1
7 101856650 intron variant G/A snv 2.2E-03 3
rs117064827
DNMT1 ; S1PR2
19 10224049 missense variant A/G;T snv 7.3E-03 1
rs140658666
S1PR2 ; DNMT1
19 10228310 intron variant CAAAACAAAACAAAA/-;CAAAA;CAAAACAAAA;CAAAACAAAACAAAACAAAA;CAAAACAAAACAAAACAAAACAAAA delins 0.14 1
rs2288937
DNMT1 ; MIR4322 ; S1PR2
19 10230236 intron variant A/C;G snv 1
rs28693921
S1PR2
19 10231337 upstream gene variant G/A;C;T snv 1
rs8113613 19 10239973 regulatory region variant C/T snv 0.15 1
rs11628569
RCOR1
14 102724025 intron variant A/G snv 0.24 1
rs7085104
BORCS7-ASMT ; AS3MT
1.000 0.040 10 102869116 intron variant A/G snv 0.35 2
rs111326718
CNNM2
10 103011454 intron variant -/TAAAA delins 0.40 1
rs7896547
NT5C2
10 103107201 intron variant A/G snv 0.41 1
rs2765041 14 103525141 non coding transcript exon variant T/A snv 0.68 1
rs12893668 14 103551456 upstream gene variant G/A snv 0.28 1
rs1654723
ANGPT1
8 107381731 intron variant A/G snv 0.48 1
rs145224266
ANGPT1
8 107388433 intron variant TAAATAAA/-;TAAA;TAAATAAATAAA delins 1
rs6040116
LINC01752
20 10739131 intron variant C/T snv 5.5E-02 1
rs60992881
NPRL3
16 107595 intron variant AAAAAAAAA/-;A;AA;AAA;AAAA;AAAAA;AAAAAA;AAAAAAA;AAAAAAAA;AAAAAAAAAA;AAAAAAAAAAA;AAAAAAAAAAAAAAA delins 0.38 2
rs9486913
FOXO3
6 108639637 intron variant C/G snv 0.20 1
rs561823900
DZIP3
3 108640397 intron variant TTTTTT/-;TT;TTTT;TTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT delins 1
rs9480866
FOXO3
6 108641439 intron variant C/T snv 0.19 1
rs932223
CCDC162P
6 109265453 intron variant T/C snv 0.51 1