Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 11
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 8
rs7335046 0.807 0.040 13 99389484 downstream gene variant G/C snv 0.80 4
rs7309332 1.000 0.040 12 7938243 upstream gene variant T/C snv 0.59 3
rs12296850 0.925 0.080 12 100426307 downstream gene variant A/G snv 8.7E-02 2
rs1412115 0.925 0.080 10 33799125 regulatory region variant T/C snv 0.58 2
rs7097008 1.000 0.040 10 67849782 non coding transcript exon variant C/A snv 0.60 1
rs9651495 1.000 0.040 10 89172624 regulatory region variant G/A snv 0.13 1
rs774121564
ACP1
1.000 0.040 2 275197 missense variant C/G snv 4.1E-06 1
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 60
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 35
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 93
rs1801166
APC
0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 16
rs1130409
APEX1
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 28
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 22
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 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-06 484
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 31
rs1048638
CA9
0.807 0.160 9 35681125 3 prime UTR variant C/A;G snv 10
rs4645978
CASP9 ; DNAJC16
0.827 0.120 1 15525539 intron variant C/A;T snv 8
rs987525
CCDC26
0.807 0.160 8 128933908 intron variant C/A snv 0.31 6