Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10036386
PDE8B
1.000 0.040 5 77247778 intron variant C/T snv 0.40 1
rs1050976
IRF4
0.851 0.280 6 408079 3 prime UTR variant C/T snv 0.37 2
rs1064191 1.000 0.040 6 31107598 downstream gene variant T/A;C snv 1
rs10759944
PTCSC2
0.925 0.080 9 97794690 intron variant A/G snv 0.72 3
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 4
rs10917477
MICOS10
1.000 0.040 1 19534612 intron variant A/C;G;T snv 1
rs10984103 0.925 0.080 9 97876993 TF binding site variant A/C snv 0.68 2
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 12
rs11066188
HECTD4
0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06 4
rs11066320
PTPN11
0.925 0.120 12 112468611 intron variant A/G snv 0.70 4
rs116909374 0.776 0.120 14 36269155 regulatory region variant C/T snv 2.3E-02 1
rs12138950
LOC105376817 ; LOC105376819 ; LOC105376818 ; MICOS10
0.925 0.040 1 19512621 intron variant A/C snv 5.4E-03 1
rs12191243 1.000 0.040 6 135125688 intergenic variant C/G snv 0.20 2
rs1382879
PDE8B
1.000 0.040 5 77226043 intron variant T/A;C snv 1
rs1443438
PTCSC2
0.827 0.080 9 97787746 intron variant T/A;C snv 3
rs1479567
PDE8B
1.000 0.040 5 77232197 intron variant G/A;C snv 1
rs17019823
VAV3
1.000 0.040 1 107727331 intron variant A/C snv 9.6E-02 1
rs17020055
VAV3
1.000 0.040 1 107793911 intron variant A/C snv 0.11 1
rs17020088
VAV3
1.000 0.040 1 107809190 intron variant T/C snv 0.15 1
rs174599
FADS2
1.000 0.040 11 61854084 intron variant G/C snv 0.47 1
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 11
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs1877432
PTCSC2
1.000 0.040 9 97781598 intron variant G/A snv 0.36 1
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 2
rs2249876 1.000 0.040 6 31080610 upstream gene variant G/A snv 0.45 1