Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs116609693
ANKRD19P
0.925 0.040 9 92811394 intron variant C/T snv 6.1E-02 2
rs1690818
CNTN5
0.925 0.040 11 99625823 intron variant C/T snv 0.61 2
rs2017122
KMT2A
0.925 0.040 11 118444134 intron variant C/T snv 4.0E-02 2
rs76767803 0.925 0.040 3 36230378 intergenic variant C/T snv 0.16 2
rs782212
LOC105378797
0.925 0.040 1 72479983 intron variant C/T snv 0.34 2
rs10514299
TMEM161B-AS1
0.827 0.120 5 88367793 intron variant C/T snv 0.21 1
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs10405744
ZNF93
0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 4
rs2302045
MTERF4 ; SNED1
0.851 0.040 2 241081801 splice region variant G/A snv 7.6E-02 1.0E-01 4
rs6586354 0.851 0.040 1 234897489 intron variant G/A snv 0.25 4
rs11591827 0.925 0.040 10 81128126 intergenic variant G/A snv 8.4E-02 3
rs11924809
DGKG
0.925 0.040 3 186353656 intron variant G/A snv 5.3E-02 3
rs143934587 0.925 0.040 20 19165806 intergenic variant G/A snv 9.1E-03 3
rs1548076 0.925 0.040 15 69934284 intergenic variant G/A snv 0.95 3
rs183124483
NLK
0.925 0.040 17 28110028 intron variant G/A snv 7.1E-04 3
rs74860738 0.925 0.040 11 80671683 intergenic variant G/A snv 7.2E-02 3
rs7555693 0.925 0.040 1 106295917 intergenic variant G/A snv 0.45 3
rs1961982
C12orf42
0.925 0.040 12 103218955 intergenic variant G/A snv 0.27 2
rs120074175
TPH2
0.827 0.080 12 72031544 missense variant G/A snv 1.2E-05 7.0E-06 1
rs1545843
LOC107984536
0.827 0.120 12 84170289 intron variant G/A snv 0.52 1
rs760161369
MTHFR
0.882 0.040 1 11800214 missense variant G/A;C snv 2.8E-05; 4.0E-06 1
rs6063349
CSE1L
0.925 0.040 20 49065345 intron variant G/A;C;T snv 3
rs17154917 0.851 0.040 7 81207393 intergenic variant G/A;T snv 4
rs6546604 0.925 0.040 2 70415675 intron variant G/A;T snv 3
rs55945116
SEC11A
0.882 0.040 15 84676882 intron variant G/C snv 0.26 4