Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 40
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 20
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 19
rs55705857
CCDC26
0.732 0.080 8 129633446 intron variant A/G snv 3.9E-02 15
rs7003908
PRKDC
0.716 0.320 8 47858141 intron variant C/A snv 0.66 15
rs11196067
VTI1A
0.752 0.160 10 112709306 intron variant A/T snv 0.32 10
rs2235544
DIO1
0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 10
rs2293157
STAT5A
0.763 0.120 17 42300657 intron variant C/A;T snv 9
rs2297440
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.080 20 63680946 intron variant T/C snv 0.81 9
rs4295627
CCDC26
0.763 0.200 8 129673211 intron variant T/G snv 0.17 9
rs11860248
RBBP6
0.882 0.040 16 24566445 intron variant T/G snv 0.27 5
rs2440472
AMFR
0.827 0.080 16 56402912 intron variant A/G snv 0.61 5
rs3092993
ATM ; C11orf65
0.827 0.040 11 108364388 intron variant C/A snv 0.11 5
rs2017309
CHEK2
0.851 0.040 22 28735438 intron variant T/A snv 0.23 4
rs8057643
RBFOX1
0.851 0.040 16 6910689 intron variant C/A;T snv 4
rs12645561
NEIL3
0.882 0.120 4 177339718 intron variant C/A;T snv 3
rs2033214
RBBP6
0.882 0.040 16 24566199 intron variant T/G snv 0.14 3
rs6470745
CCDC26
0.882 0.040 8 129629675 intron variant A/G snv 0.18 3
rs891835
CCDC26
0.851 0.120 8 129479506 intron variant T/G snv 0.17 3
rs10464870
CCDC26
0.882 0.040 8 129465577 intron variant C/T snv 0.80 2
rs11979158
EGFR
0.882 0.040 7 55091656 intron variant A/G;T snv 0.20 2
rs12230172
LOC105369844
0.882 0.040 12 75848895 intron variant A/G snv 0.48 2
rs2291427
ALOX5
0.925 0.040 10 45440776 intron variant A/G;T snv 2
rs3851634
POLR3B
0.882 0.040 12 106419124 intron variant T/C snv 0.22 2
rs7325927
FAM155A-IT1 ; FAM155A
0.925 0.040 13 107823165 intron variant C/T snv 0.38 2