Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 12
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 11
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
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs1857231 1.000 0.080 10 8919651 intergenic variant G/A snv 0.64 1
rs6499100 1.000 0.080 16 52797550 intergenic variant T/C snv 0.42 1
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 1
rs7982677
GPC5
1.000 0.080 13 92336070 intron variant C/A snv 0.29 1
rs4771856
GPC5 ; GPC5-AS2
1.000 0.080 13 92342256 intron variant C/A snv 0.29 1
rs2388896
LINC02676
1.000 0.080 10 8912261 intron variant A/G snv 0.64 1
rs2228638
NRP1
1.000 0.080 10 33186354 missense variant C/T snv 0.12 9.4E-02 1
rs233716
RPH3A
1.000 0.080 12 112602139 intron variant C/T snv 0.58 1
rs233722
RPH3A
1.000 0.080 12 112593670 intron variant G/A snv 0.53 1