Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3745601
P2RY11 ; PPAN-P2RY11
0.882 0.120 19 10113872 missense variant G/A snv 0.16 0.13 3
rs1050286
OLR1
0.882 0.160 12 10158964 3 prime UTR variant T/C snv 0.40 3
rs3736235
OLR1
0.925 0.080 12 10160476 non coding transcript exon variant T/C snv 0.43 0.40 2
rs11053646
OLR1
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs200478651
F7
1.000 0.080 13 113118414 splice region variant C/A;T snv 8.4E-06; 2.1E-05 1
rs1183027238
F7
1.000 0.080 13 113118480 synonymous variant C/T snv 1
rs201058276
F7
0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 11
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs12375498
PAPPA
1.000 0.080 9 116187719 synonymous variant C/T snv 0.19 0.17 1
rs13290387
PAPPA
0.925 0.120 9 116227647 intron variant G/C snv 0.54 2
rs1191926239
TLR4
0.807 0.200 9 117704539 missense variant C/G snv 4.0E-06 7
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1255283120
MTHFR
0.807 0.160 1 11792345 missense variant G/A snv 4.0E-06 7.0E-06 7
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1217035505
P2RX7 ; LOC105370032
1.000 0.080 12 121184674 missense variant G/A snv 1
rs775913429
P2RX2
1.000 0.080 12 132620455 missense variant G/A snv 8.0E-06 1.4E-05 1
rs2804924
LOC105374937 ; SIRT5
1.000 0.080 6 13574110 upstream gene variant G/A;C;T snv 1
rs112443954
SIRT5 ; LOC105374937
1.000 0.080 6 13574259 upstream gene variant G/C snv 0.27 1
rs767830104
CXCR4
0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs4636297
EGFL7 ; MIR126
0.724 0.360 9 136670698 intron variant A/G snv 0.67 0.65 14
rs1140713
MIR126 ; EGFL7
1.000 0.080 9 136670833 intron variant C/T snv 0.13 1