Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10184428 2 164155317 intron variant C/A;G snv 5
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 5
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 5
rs13149993 4 80237391 regulatory region variant G/A;C snv 5
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 5
rs35443 12 115115073 intergenic variant G/C snv 0.40 5
rs35444 12 115114632 intergenic variant A/G snv 0.38 5
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs4409766
BORCS7-ASMT ; BORCS7
1.000 0.040 10 102856906 intron variant T/C snv 0.14 5
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 5
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 5
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv 5
rs2067087
HOTTIP ; HOXA13
1.000 0.080 7 27202041 non coding transcript exon variant G/C;T snv 5
rs1275988
KCNK3
1.000 0.080 2 26691496 upstream gene variant C/T snv 0.48 5
rs1731249
KCNK3
2 26697157 intron variant T/A snv 0.48 5
rs4980389
LSP1
11 1871355 5 prime UTR variant G/A snv 0.35 5
rs6021247
NFATC2
1.000 0.080 20 51492442 intron variant G/A snv 0.65 5
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs167479
RGL3
19 11416089 missense variant T/A;C;G snv 5
rs16896398
SLC22A7
6 43294966 upstream gene variant A/T snv 0.42 5
rs8068318
TBX2
17 61406405 non coding transcript exon variant C/T snv 0.56 5
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 5
rs3790604
WNT2B
1 112504257 intron variant C/A snv 7.8E-02 5
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 4