Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2293479
AP4M1
1.000 0.080 7 100106335 intron variant T/C;G snv 0.29; 4.0E-06 1
rs4727449
STAG3 ; CASTOR3
1.000 0.080 7 100188127 intron variant C/T snv 0.11 1
rs866500
CASTOR3
1.000 0.080 7 100242838 intron variant A/G;T snv 1
rs858502
CASTOR3
1.000 0.080 7 100245730 intron variant T/C snv 0.50 1
rs35305377
STAG3L5P ; PMS2P1 ; STAG3L5P-PVRIG2P-PILRB
1.000 0.080 7 100341332 intron variant G/A snv 0.56 1
rs2289506
NIT2
1.000 0.080 3 100346058 non coding transcript exon variant C/T snv 0.24 1
rs1859788
PILRA
0.925 0.080 7 100374211 missense variant A/C;G snv 4.0E-06; 0.65 1
rs1476679
ZCWPW1
0.925 0.080 7 100406823 intron variant C/A;T snv 4.0E-06; 0.74 1
rs117969561
GGACT
1.000 0.080 13 100558935 intron variant C/T snv 2.5E-02 1
rs2734897
AGFG2
1.000 0.080 7 100561944 intron variant A/G snv 0.74 1
rs2970989 1.000 0.080 2 100697607 intergenic variant T/G snv 0.18 1
rs1399439
ANO4
1.000 0.080 12 100827461 intron variant A/G snv 3.7E-02 1
rs1774093 1.000 0.080 9 101884874 intergenic variant A/G snv 0.12 1
rs115641191 1.000 0.080 4 102133052 intergenic variant C/T snv 6.2E-03 1
rs2852894 1.000 0.080 11 102284743 intergenic variant A/G snv 0.93 1
rs7840202
UBR5
0.851 0.160 8 102296172 intron variant A/C snv 0.21 1
rs972936
IGF1 ; LINC02456
0.807 0.200 12 102431143 intron variant T/C snv 0.70 3
rs3824755
CYP17A1
0.925 0.120 10 102836092 intron variant G/A;C;T snv 2
rs573521 1.000 0.080 11 102846249 upstream gene variant A/G snv 0.57 1
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs12808148
MMP12
1.000 0.080 11 102862432 downstream gene variant T/C snv 0.12 1
rs6468852
AZIN1-AS1
1.000 0.080 8 102963761 intron variant A/G snv 0.30 1
rs76070545 1.000 0.080 8 103359219 intergenic variant T/C snv 3.6E-02 1
rs111278892
CNN2 ; ABCA7
1.000 0.080 19 1039324 upstream gene variant C/G;T snv 0.12 1
rs3795065
ABCA7 ; CNN2
1.000 0.080 19 1039445 upstream gene variant C/G;T snv 1