Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2001389
SUFU
0.925 0.120 10 102615501 intron variant G/A;C snv 3
rs2027605
BACH1
1.000 0.120 21 29354452 intron variant A/G snv 0.48 3
rs2235108
TRIB1
0.925 0.120 8 125436547 3 prime UTR variant G/A snv 0.25 3
rs2980879 0.925 0.120 8 125469233 intron variant A/T snv 0.69 3
rs397507851
BRCA2
0.925 0.120 13 32340761 frameshift variant AAATGTT/- delins 3
rs4269383
LOC105378072 ; LOC101928923
0.882 0.120 6 155876368 intergenic variant A/G snv 0.37 3
rs757748401
NFATC2
0.925 0.120 20 51542465 missense variant C/A;T snv 5.2E-06 3
rs876659900
PMS2
0.925 0.120 7 5982861 stop gained G/A snv 3
rs1034925236
NR5A2
0.925 0.120 1 200048258 missense variant G/C snv 2
rs10500715
SBF2
0.925 0.120 11 9951515 intron variant T/G snv 0.39 2
rs10887710 0.925 0.120 10 80270029 downstream gene variant T/C snv 0.19 2
rs11085754
SMARCA4
0.925 0.120 19 11017920 intron variant A/G snv 0.41 2
rs1153280
BACH1
1.000 0.120 21 29305751 intron variant G/A snv 0.52 2
rs11644043
BRD7
0.925 0.120 16 50327466 intron variant T/C snv 0.24 2
rs1235228469
PIK3CB
0.925 0.120 3 138684714 missense variant C/A snv 8.0E-06 2
rs12362504
SBF2 ; LOC101928008
0.925 0.120 11 9907995 intron variant T/C snv 0.37 2
rs12456874
LDLRAD4
0.925 0.120 18 13366863 intron variant A/G snv 0.20 2
rs1276300653
CAMK1 ; OGG1
0.925 0.120 3 9757072 missense variant T/C snv 7.0E-06 2
rs12939944
MAP2K4
0.925 0.120 17 12056502 intron variant C/T snv 0.45 2
rs1318
LOC101928045 ; PITPNC1
0.925 0.120 17 67695266 3 prime UTR variant A/G snv 0.30 2
rs13303010
KLHL17 ; NOC2L
0.925 0.120 1 959193 intron variant G/A snv 0.82 0.69 2
rs1336539869
CDK4
0.925 0.120 12 57751681 missense variant C/G snv 2
rs1339638227
CDKN2A
0.925 0.120 9 21971119 missense variant T/C snv 4.3E-06 2
rs138147246
OGG1
0.925 0.120 3 9756551 synonymous variant A/G snv 8.0E-06 1.4E-05 2
rs139632793
OGG1
0.925 0.120 3 9751114 missense variant G/C snv 5.2E-05 1.7E-04 2