Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3731861
PNKD ; CATIP-AS2
0.776 0.080 2 218326533 intron variant T/C snv 0.32 10
rs13020391
LOC105373881 ; PNKD
0.790 0.080 2 218319713 intron variant C/T snv 0.32 9
rs992157
TMBIM1 ; PNKD
0.790 0.080 2 218290058 5 prime UTR variant G/A snv 0.46 9
rs145013566
PNKD
2 218297998 intron variant -/C ins 5
rs2382817
PNKD ; TMBIM1
0.925 0.040 2 218286495 5 prime UTR variant A/C snv 0.61 3
rs1870125
LOC105373881 ; PNKD
2 218323178 5 prime UTR variant C/G;T snv 2
rs1877712
PNKD
2 218303709 intron variant G/A snv 0.43 2
rs4674280
PNKD ; TMBIM1
2 218276735 intron variant C/G snv 0.50 2
rs2292553
PNKD ; TMBIM1 ; MIR6513
2 218282080 missense variant G/A snv 0.55 0.43 2
rs897877
CATIP-AS2 ; PNKD
2 218328032 intron variant G/A snv 0.49 1
rs34001204
LOC105373880 ; PNKD ; LOC105373881
2 218314933 intron variant A/- del 0.44 1
rs1017698
LOC105373881 ; PNKD
2 218305802 intron variant G/A;C snv 1
rs10716631
PNKD
2 218273447 intron variant T/G snv 1
rs1870123
PNKD ; LOC105373881
2 218322975 intron variant G/A;C snv 1
rs2271543
PNKD ; TMBIM1
2 218277768 intron variant C/T snv 0.35 1
rs2382818
PNKD ; TMBIM1
2 218291184 intron variant A/T snv 0.36 1
rs4791
TMBIM1 ; PNKD
2 218274217 3 prime UTR variant C/T snv 0.44 1