Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12076373
AKT3
1.000 0.040 1 243688645 intron variant G/C snv 0.20 2
rs34988193
ANKDD1A
1.000 0.040 15 64943580 missense variant A/G snv 0.31 0.28 2
rs117677079
ANXA5
0.882 0.040 4 121673909 intron variant T/C snv 8.3E-03 3
rs1131239
ANXA5
1.000 0.040 4 121696590 5 prime UTR variant G/A;C;T snv 0.12 0.17 1
rs145619195
ANXA5
1.000 0.040 4 121674585 intron variant T/C snv 9.4E-04 1
rs2306415
ANXA5
1.000 0.040 4 121696476 intron variant C/G snv 0.16 1
rs2306420
ANXA5
1.000 0.040 4 121670320 intron variant G/A snv 0.21 1
rs41278075
ANXA5
1.000 0.040 4 121669758 intron variant G/A snv 0.23 0.18 1
rs3092993
ATM ; C11orf65
0.827 0.040 11 108364388 intron variant C/A snv 0.11 5
rs1044129
AVEN ; RYR3
0.790 0.200 15 33866065 3 prime UTR variant A/G;T snv 9
rs2279115
BCL2
0.724 0.320 18 63319604 5 prime UTR variant G/A;T snv 18
rs762541432
BDNF-AS ; BDNF
1.000 0.040 11 27657901 missense variant T/C snv 4.0E-06 1
rs17655
BIVM-ERCC5 ; ERCC5
0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs7572263
C2orf80
1.000 0.040 2 208186862 intron variant A/G snv 0.27 2
rs1045485
CASP8
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs1052576
CASP9
0.807 0.200 1 15506048 missense variant T/A;C snv 0.53 9
rs55705857
CCDC26
0.732 0.080 8 129633446 intron variant A/G snv 3.9E-02 16
rs4295627
CCDC26
0.763 0.200 8 129673211 intron variant T/G snv 0.17 11
rs891835
CCDC26
0.851 0.120 8 129479506 intron variant T/G snv 0.17 5
rs10464870
CCDC26
0.882 0.040 8 129465577 intron variant C/T snv 0.80 3
rs6470745
CCDC26
0.882 0.040 8 129629675 intron variant A/G snv 0.18 3
rs12544799
CCDC26
1.000 0.040 8 129651264 intron variant A/G snv 0.34 1
rs16904140
CCDC26
1.000 0.040 8 129653397 intron variant G/A snv 0.19 1