Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057941
GBAP1
0.701 0.280 1 155216951 non coding transcript exon variant G/A;T snv 0.46 18
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21 17
rs186507655 0.708 0.280 1 1351675 upstream gene variant G/A snv 6.8E-03 17
rs2974935
MTX1
0.708 0.280 1 155212052 non coding transcript exon variant G/A;C;T snv 17
rs34517439
DNAJB4 ; GIPC2
0.882 0.120 1 77984833 intron variant C/A snv 7.3E-02 7
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs17391694 0.882 0.120 1 78157942 regulatory region variant C/T snv 7.8E-02 5
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 4
rs71658797
AK5
0.925 0.080 1 77501822 intron variant T/A snv 7.3E-02 3
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 2
rs34585985 0.925 0.080 1 210316066 intergenic variant A/G snv 5.2E-02 2
rs9651118
MTHFR
0.683 0.480 1 11802157 intron variant T/C snv 0.18 2
rs10436951
CEP170
1.000 0.080 1 243199378 intron variant A/G snv 7.1E-02 1
rs144503462
LINC01347 ; SEPTIN14P21
1.000 0.080 1 243029970 intron variant T/C snv 2.8E-02 1
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 1
rs71641308
ZZZ3
1.000 0.080 1 77621033 intron variant C/A;G;T snv 1
rs71641333
MGC27382
1.000 0.080 1 78277321 intron variant T/A snv 4.1E-02 1
rs7534220
RTCA-AS1
1.000 0.080 1 100258911 non coding transcript exon variant T/A;C snv 1
rs77045810 1.000 0.080 1 168535779 downstream gene variant A/C snv 0.10 1
rs78062588
ADAR
1.000 0.080 1 154593749 intron variant T/C snv 5.1E-02 1
rs1800440
CYP1B1
0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 6
rs2070959
UGT1A8 ; UGT1A7 ; UGT1A9 ; UGT1A10 ; UGT1A6
0.742 0.320 2 233693545 missense variant A/G snv 0.31 0.30 3
rs5742933
ORMDL1 ; PMS1
0.882 0.080 2 189784590 5 prime UTR variant G/A;C snv 2