Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7955371
WNK1
12 885321 missense variant G/C snv 1.00 0.99 1
rs556766
PIGO
9 35089051 3 prime UTR variant A/C snv 1.00 0.98 1
rs649964
KL
13 33061698 missense variant T/A;C snv 8.0E-06; 0.99 3
rs6670122
MRPL24
0.882 0.120 1 156737983 intron variant T/C;G snv 0.99 1
rs4838544
CHAT
10 49648606 missense variant G/A;T snv 0.99; 1.2E-05 2
rs669661
PRG3
11 57380702 missense variant A/G snv 0.99 0.96 1
rs480392
NTNG1
1 107436774 synonymous variant A/C snv 0.99 0.95 3
rs2809270
ZFAND5
9 72360220 splice region variant T/A;C snv 0.99 2
rs2756231
SORCS1
10 106706654 intron variant C/T snv 0.98 0.97 1
rs4682484
CFAP44
3 113304023 missense variant T/A;C snv 0.98 1
rs7105056
BCO2
11 112193708 non coding transcript exon variant T/C snv 0.97 0.95 1
rs10800427
NME7
1 169303213 non coding transcript exon variant A/C;T snv 0.96 1
rs10800428
NME7
1 169303215 non coding transcript exon variant G/A;T snv 0.96 1
rs643507
LPIN2 ; CHORDC1P4
1.000 0.080 18 2946293 non coding transcript exon variant C/T snv 0.96 0.92 1
rs3132453
PRRC2A
0.925 0.200 6 31636267 missense variant T/G snv 0.96 0.95 1
rs6784615
NISCH
1.000 0.080 3 52472410 intron variant C/T snv 0.96 0.96 1
rs3130253
MOG
0.925 0.120 6 29666235 missense variant A/G;T snv 0.95; 4.1E-06 1
rs505151
PCSK9
0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 3
rs2327089
PLCB1
1.000 0.080 20 8788533 splice region variant C/T snv 0.95 0.90 1
rs7698623
MEPE
4 87834676 intron variant T/A;C snv 6.1E-05; 0.94 1
rs619865
MMP24-AS1-EDEM2 ; MMP24OS ; EIF6
1.000 0.040 20 35279894 intron variant A/G snv 0.94 0.94 1
rs6009
F5
1.000 0.080 1 169529596 intron variant T/A;C snv 0.94 3
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs629001
MYBPHL
1 109296296 missense variant C/G;T snv 0.93 3
rs12341266
RGS3
1.000 0.040 9 113594236 missense variant A/C;G snv 0.93 1