Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1452075
CADPS
1.000 0.040 3 62495388 intron variant C/T snv 0.73 4
rs1800692
TNFRSF1A
0.925 0.120 12 6333180 missense variant A/G snv 0.64 0.71 1
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 3
rs4141463
MACROD2
0.925 0.040 20 14766825 intron variant T/C snv 0.50 1
rs7794745
CNTNAP2
0.851 0.040 7 146792514 intron variant A/T snv 0.49 1
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs2289195
DNMT3A
1.000 0.040 2 25240614 intron variant G/A snv 0.41 0.41 1
rs1858830
MET
0.925 0.040 7 116672385 5 prime UTR variant C/G snv 0.40 1
rs2388334 0.882 0.040 6 98143746 intron variant A/G snv 0.39 5
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 1
rs13294439 1.000 0.040 9 23358877 intron variant A/C snv 0.32 2
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 6
rs11787216 1.000 0.040 8 141605122 intron variant C/T snv 0.26 2
rs3756963
ELOVL2
0.882 0.200 6 11021921 intron variant T/C snv 0.24 1
rs2898883
PHB
1.000 0.040 17 49405591 intron variant G/A snv 0.23 2
rs6824295
STX18-AS1
0.851 0.120 4 4612553 intron variant C/T snv 0.20 1
rs16835979
STX18-AS1
0.851 0.120 4 4633549 intron variant C/A snv 0.20 1
rs9468304
ELOVL2-AS1 ; ELOVL2
1.000 0.040 6 11041932 intron variant G/A snv 0.19 1
rs10498676
ELOVL2
0.925 0.040 6 11026766 intron variant G/A snv 0.18 1
rs7341475
RELN
0.851 0.240 7 103764368 intron variant G/A snv 0.17 2
rs17606561
ELOVL2
1.000 0.040 6 10982126 3 prime UTR variant G/A snv 0.17 1
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs2230365
NFKBIL1
0.925 0.160 6 31557671 synonymous variant C/T snv 0.16 0.13 2
rs4534
GML ; CYP11B1
0.925 0.240 8 142879686 missense variant C/T snv 8.4E-02 4.1E-02 1
rs16976358
LINC00907
0.827 0.080 18 42611606 intron variant T/C snv 1.0E-02 1