Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2017309
CHEK2
0.851 0.040 22 28735438 intron variant T/A snv 0.23 4
rs28357681
ND6 ; CYTB
0.851 0.040 MT 14798 missense variant T/C snv 4
rs375391381
FRMD5
0.851 0.040 15 43883735 missense variant C/T snv 8.0E-06 1.4E-05 4
rs572480837
POU5F1 ; TCF19
0.851 0.040 6 31165582 missense variant T/A snv 5.0E-04 8.4E-05 4
rs755794544
PDGFA
0.851 0.040 7 512435 missense variant T/C snv 4.0E-06 4
rs757066045
CDKN2A
0.882 0.040 9 21974725 missense variant C/T snv 8.2E-06 4
rs760090729
H3C10
0.851 0.040 6 27810468 missense variant G/A snv 4
rs766265850
MIR4640 ; DDR1
0.851 0.040 6 30889239 missense variant G/A snv 8.1E-06 7.0E-06 4
rs8057643
RBFOX1
0.851 0.040 16 6910689 intron variant C/A;T snv 4
rs866960721
H3C4
0.851 0.040 6 26196856 missense variant C/G;T snv 4.0E-06 4
rs13332653 0.882 0.040 16 24578078 intergenic variant T/G snv 0.11 3
rs1346787
EFEMP1 ; LOC112268416
0.882 0.040 2 55865477 downstream gene variant C/A;G;T snv 3
rs1801591
ETFA
0.882 0.040 15 76286421 missense variant G/A snv 7.4E-02 6.4E-02 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
rs863225401
MSH6 ; FBXO11
0.925 0.040 2 47799866 stop gained G/A snv 3
rs879254044
MSH2
0.925 0.040 2 47475148 missense variant G/A;C;T snv 3
rs9933544 0.882 0.040 16 24576962 downstream gene variant A/C snv 0.29 3
rs10464870
CCDC26
0.882 0.040 8 129465577 intron variant C/T snv 0.80 2
rs11548193
BCAT2
0.925 0.040 19 48799813 missense variant G/A;C snv 0.14 2
rs11558961
GFAP
0.925 0.040 17 44907319 3 prime UTR variant G/C;T snv 0.27; 1.2E-05 2
rs11670188
BTBD2
0.925 0.040 19 2014038 non coding transcript exon variant A/G snv 0.16 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
rs1435266782
IDH2
0.925 0.040 15 90088633 missense variant C/A;T snv 4.0E-06 2