Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1554700718
HNRNPK
0.658 0.360 9 83975540 non coding transcript exon variant T/C snv 59
rs1555743003
ASXL3
0.701 0.520 18 33740444 splice donor variant G/A snv 58
rs1554317002
LOC112267983 ; CDK13
0.724 0.440 7 39950821 frameshift variant C/- delins 45
rs864321670
ALDH18A1
0.763 0.320 10 95633012 missense variant C/T snv 24
rs387906846
ARID1A
0.807 0.280 1 26773716 stop gained C/G;T snv 19
rs111854391
TGFBR1
0.716 0.280 9 99138006 stop gained C/A;T snv 4.0E-06 18
rs1443187318
AEBP1
0.882 0.080 7 44108060 stop gained -/A delins 1.3E-05 14
rs137854461
FBN1
0.790 0.280 15 48437026 missense variant T/C snv 12
rs121913528
KRAS
0.851 0.160 12 25227349 missense variant C/A;T snv 12
rs397515804
FBN1
0.776 0.200 15 48472628 missense variant C/A;T snv 11
rs140291094
STAC3
0.742 0.320 12 57244322 missense variant C/G snv 9.1E-05 3.8E-04 11
rs113812345
FBN1
0.790 0.160 15 48513591 stop gained G/A snv 10
rs1555398397
FBN1
0.807 0.240 15 48485436 missense variant C/T snv 10
rs397515789
FBN1
0.776 0.240 15 48488112 splice donor variant C/A;T snv 10
rs771866012
CHST3
0.882 0.080 10 72007522 missense variant C/G;T snv 4.2E-06; 4.2E-06 8
rs1316347883
CHST3
0.851 0.080 10 72007935 missense variant G/A;C snv 6.9E-06 4
rs2272515
LOC100130701 ; FSTL1
0.882 0.080 3 120416036 intron variant T/C snv 0.36 0.34 3