Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10177758
PLCL1
2 197994193 intron variant A/G snv 0.48 1
rs10178214
IL1RL2
2 102242461 downstream gene variant G/T snv 0.24 1
rs10181785 2 102408814 upstream gene variant C/T snv 0.22 1
rs10184227
PLCL1
2 198029581 intron variant C/T snv 0.48 1
rs10184395
PLCL1
2 198029561 intron variant G/A snv 0.69 1
rs10189897
PLCL1
2 197948686 intron variant A/G;T snv 1
rs10190226
PLCL1
2 198036840 intron variant C/T snv 0.69 1
rs10192466
PLCL1
2 197873295 intron variant G/A;C snv 1
rs10196612
PLCL1
2 198029415 intron variant T/C snv 0.49 1
rs10196961
RFTN2
2 197649206 intron variant G/A snv 0.47 1
rs10197310 2 102403570 downstream gene variant T/A snv 0.22 1
rs10198606
PLCL1
2 197905015 intron variant C/A;G;T snv 1
rs10202813 2 102403280 downstream gene variant G/T snv 0.22 1
rs10206714
PLCL1
2 198041757 intron variant C/A;T snv 1
rs10207433
PLCL1
2 197941206 intron variant G/T snv 0.51 1
rs10210006
LINC00299
2 8326356 intron variant C/G snv 0.29 1
rs10210176 2 102463056 intergenic variant C/A snv 0.22 1
rs1022804
TTC6
14 37711608 intron variant G/A snv 0.20 1
rs1031163 10 9015459 regulatory region variant G/T snv 0.33 1
rs1035765
LPP
3 188402995 intron variant A/T snv 0.38 1
rs1035766
LPP
3 188402952 intron variant G/A snv 0.38 1
rs1036333
PLCL1
2 198079063 intron variant G/T snv 0.51 1
rs1044265
EMSY
11 76551084 3 prime UTR variant A/G snv 0.40 1
rs10447257 5 110845538 intergenic variant T/C;G snv 1
rs10470854 4 38766912 intergenic variant A/G snv 0.40 1