Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17278665
EFEMP1 ; LOC112268416
1.000 0.040 2 55868859 intron variant C/G snv 0.13 1
rs727139
KCNH8
1.000 0.040 3 19293203 intron variant A/G snv 0.13 1
rs2030136
SKAP2
1.000 0.040 7 26851397 intron variant T/C snv 0.21 1