Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1564483
BCL2
1.000 0.080 18 63127421 3 prime UTR variant C/T snv 0.22 4
rs112295309
SCRIB ; MIR937
1.000 0.080 8 143813896 missense variant T/C;G snv 6.1E-04 3
rs121913430
EGFR
1.000 0.080 7 55174740 missense variant G/A snv 3
rs41281081
MET
1.000 0.080 7 116796211 3 prime UTR variant G/A snv 2.5E-03 3
rs76322625
MET
1.000 0.080 7 116798111 3 prime UTR variant C/A;T snv 3
rs915894
NOTCH4
1.000 0.080 6 32222613 missense variant T/G snv 0.35 0.36 3
rs1048977
CDA
1.000 0.080 1 20618562 synonymous variant C/T snv 0.31 0.34 2
rs10503380 1.000 0.080 8 9552985 upstream gene variant C/T snv 0.25 2
rs11466345
TGFB1
1.000 0.080 19 41337556 intron variant T/C snv 0.12 2
rs11622887
SYNE3
1.000 0.080 14 95476110 upstream gene variant A/C snv 0.52 2
rs11632964
SMAD3
1.000 0.080 15 67071235 intron variant C/G;T snv 2
rs11991621 1.000 0.080 8 9549072 intergenic variant C/T snv 0.18 2
rs1213277193
ROS1
1.000 0.080 6 117359856 missense variant C/T snv 1.4E-05 2
rs121913231
EGFR
1.000 0.080 7 55174794 missense variant C/T snv 8.0E-06 2
rs12541709
TNKS
1.000 0.080 8 9751081 intron variant C/G snv 0.29 2
rs12621220 1.000 0.080 2 112840678 non coding transcript exon variant C/T snv 0.24 2
rs13398721
LOC101928196 ; LOC105373458
1.000 0.080 2 19429543 intergenic variant T/C snv 0.21 2
rs16950650
ABCC4
1.000 0.080 13 95123178 intron variant C/T snv 4.7E-02 2
rs17635492 1.000 0.080 6 117450114 intron variant A/T snv 2.4E-02 2
rs201661522
ABCB1
1.000 0.080 7 87539293 missense variant A/G snv 6.4E-05 1.0E-04 2
rs2018683 1.000 0.080 7 28974579 intergenic variant G/A;T snv 2
rs228644
PER3
1.000 0.080 1 7806023 intron variant G/A snv 0.36 2
rs2305035
CBLB
1.000 0.080 3 105720182 synonymous variant G/A snv 0.22 0.21 2
rs344924 1.000 0.080 1 67639770 intergenic variant A/G snv 0.17 2
rs397516979
ERBB2 ; MIR4728
1.000 0.080 17 39724744 protein altering variant -/TCT;TGT;TTT ins 2