Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11979158
EGFR
0.882 0.040 7 55091656 intron variant A/G;T snv 0.20 5
rs1920116
LRRC31
0.882 0.040 3 169862183 intron variant G/A snv 0.25 5
rs75061358 0.882 0.040 7 54848587 intergenic variant T/C;G snv 4
rs59060240
EGFR
0.882 0.040 7 55080369 intron variant AA/-;A;AAA;AAAA;AAAAAAAAAAA delins 4
rs723527
EGFR
0.882 0.040 7 55067179 intron variant A/G snv 0.53 4
rs1801591
ETFA
0.882 0.040 15 76286421 missense variant G/A snv 7.4E-02 6.4E-02 4
rs10852606
HEATR3
0.882 0.040 16 50094961 intron variant T/A;C snv 4
rs1805389
LIG4
0.882 0.080 13 108211261 missense variant G/A;C;T snv 5.7E-02; 4.1E-06 4
rs3751667
LMF1
1.000 0.040 16 954554 synonymous variant C/T snv 0.28 0.29 4
rs12230172
LOC105369844
0.882 0.040 12 75848895 intron variant A/G snv 0.48 4
rs11233250
MIR4300HG
0.882 0.040 11 82685972 intron variant C/T snv 0.11 4
rs3851634
POLR3B
0.882 0.040 12 106419124 intron variant T/C snv 0.22 4
rs12752552
RAVER2
0.882 0.040 1 64763616 intron variant T/C snv 0.13 4
rs2562152
RHBDF1
0.882 0.040 16 73898 intron variant A/T snv 0.67 4
rs2235573
SLC16A8
0.882 0.040 22 38081923 synonymous variant G/A snv 0.47 0.46 4
rs648044
ZBTB16 ; LOC101928875
0.882 0.040 11 114160077 non coding transcript exon variant A/G;T snv 4
rs12021720
DBT
0.925 0.160 1 100206504 missense variant T/A;C snv 0.92 3
rs63750790
MSH2
1.000 0.160 2 47476425 missense variant G/A snv 3.2E-05 7.0E-06 3
rs12088062 1.000 0.040 1 244811284 intergenic variant C/T snv 0.20 2
rs1409785 1.000 0.040 1 74782438 intergenic variant G/A snv 0.65 2
rs16838813 1.000 0.040 1 4364085 intergenic variant G/A;T snv 0.11 2
rs17110757
ACOT11
1.000 0.040 1 54584133 intron variant G/A snv 0.20 2
rs10131032
AKAP6
1.000 0.040 14 32780875 intron variant G/A snv 9.3E-02 2
rs12076373
AKT3
1.000 0.040 1 243688645 intron variant G/C snv 0.20 2
rs7572263
C2orf80
1.000 0.040 2 208186862 intron variant A/G snv 0.27 2