Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs758272654
GNAS
0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs1136201
ERBB2
0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs13387042
LOC105373874 ; LOC101928278
0.732 0.280 2 217041109 intergenic variant A/G snv 0.44 16
rs12951053
TP53
0.732 0.160 17 7674089 intron variant A/C snv 0.10 14
rs74315364
RNASEL
0.732 0.200 1 182586014 stop gained C/A snv 3.6E-03; 4.0E-06 3.3E-03 13
rs1625895
TP53
0.752 0.200 17 7674797 non coding transcript exon variant T/A;C;G snv 9.1E-06; 0.86; 4.5E-06 13
rs28997576
BARD1
0.776 0.160 2 214752454 missense variant C/G;T snv 1.5E-02 11
rs744154
ERCC4
0.763 0.280 16 13921224 intron variant G/C snv 0.23 11
rs796065354
ESR1
0.882 0.080 6 151944320 missense variant A/G snv 9
rs2016347
IGF1R
0.790 0.160 15 98960571 3 prime UTR variant G/A;T snv 9
rs12947788
TP53
0.776 0.280 17 7674109 intron variant G/A snv 0.10 8
rs17822931
ABCC11
0.827 0.080 16 48224287 missense variant C/G;T snv 4.0E-06; 0.22 0.13 7
rs4778137
OCA2
0.827 0.080 15 28082689 intron variant C/A;G snv 6
rs786202998
BRCA1
0.851 0.080 17 43091030 stop gained C/A;T snv 5
rs1462893414
ESR1
0.882 0.080 6 151944323 missense variant A/G snv 4.0E-06 7.0E-06 5
rs965384857
LPL
0.827 0.160 8 19954234 missense variant G/A snv 4.0E-06 5
rs2909430
TP53
0.827 0.200 17 7675327 5 prime UTR variant C/G;T snv 5
rs9894946
TP53
0.925 0.160 17 7667762 intron variant A/C;G snv 2
rs1131532
TNFSF10
1.000 0.080 3 172506513 missense variant A/C;G;T snv 2.1E-05; 0.65 1