Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs141708090
C3orf20
1.000 0.120 3 14761602 missense variant G/T snv 1.9E-03 5.2E-04 1
rs2066865
FGG
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 10
rs936094
RXFP1
1.000 0.120 4 158523162 intron variant T/A;C;G snv 1
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs359312
ST8SIA6
1.000 0.120 10 17346144 intron variant C/T snv 3.6E-02 1
rs34531324
LINC01411
1.000 0.120 5 174435441 intron variant A/T snv 0.16 3
rs1135401746
GNB1
0.827 0.400 1 1806512 missense variant C/G snv 7
rs10949482
NHLRC1
1.000 0.120 6 18121083 3 prime UTR variant C/T snv 6.8E-02 1
rs1142345
TPMT
0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 9
rs79050301
TPMT
1.000 0.120 6 18151959 intron variant T/C snv 4.5E-02 1
rs2036914
F11
0.882 0.160 4 186271327 intron variant T/C snv 0.57 5
rs17505102
TP63
1.000 0.120 3 189683987 intron variant G/C snv 9.7E-02 1
rs920590 1.000 0.120 8 19793650 regulatory region variant T/C snv 0.39 3
rs1569175 1.000 0.120 2 200157231 intergenic variant T/C snv 0.88 1
rs4553808
CTLA4
0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16 28
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs2390536
SP4
1.000 0.120 7 21445779 intron variant G/A snv 0.26 1
rs3731217
CDKN2A
0.763 0.320 9 21984662 intron variant A/C;T snv 10
rs2069426
CDKN2B ; CDKN2B-AS1
1.000 0.120 9 22006274 intron variant G/A;C;T snv 4.4E-06; 4.4E-06; 7.5E-02 1
rs4266962 1.000 0.120 10 22052645 intergenic variant C/G;T snv 1
rs4748793 0.851 0.120 10 22194082 intergenic variant A/G snv 0.18 4
rs7901152
PIP4K2A
1.000 0.120 10 22544224 intron variant G/A snv 0.66 1
rs11013046
PIP4K2A
1.000 0.120 10 22551654 intron variant C/T snv 0.55 1
rs4748813
PIP4K2A
1.000 0.120 10 22557806 intron variant T/A;C snv 1
rs7088318
PIP4K2A
0.851 0.120 10 22564019 intron variant C/A snv 0.55 4