Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913322
STK11
0.882 0.120 19 1221320 missense variant C/A;G;T snv 2.9E-05; 1.2E-04 4
rs185229225
BOD1L1
0.851 0.120 4 13607505 intron variant T/C snv 4
rs10088218
LINC00824
0.851 0.120 8 128531703 intron variant G/A snv 0.13 3
rs11782652
CHMP4C
0.851 0.120 8 81741409 intron variant A/G snv 6.6E-02 3
rs121964872
CDH1
0.882 0.120 16 68833362 missense variant A/G snv 4.4E-05 1.1E-04 3
rs2072590
HAGLR ; HAGLROS
0.851 0.120 2 176177905 non coding transcript exon variant A/C;T snv 3
rs28933370
MIR4728 ; ERBB2
0.882 0.120 17 39725125 missense variant A/G snv 7.0E-06 3
rs7651446
TIPARP
0.882 0.120 3 156689208 intron variant G/T snv 7.9E-02 3
rs80356993
BRCA1
0.925 0.120 17 43063937 missense variant A/G;T snv 3
rs9303542
SKAP1
0.882 0.120 17 48334138 intron variant A/G snv 0.34 3
rs1064795649
BRIP1
1.000 0.120 17 61799205 frameshift variant CT/- delins 2
rs137852691
OPCML
0.925 0.120 11 132657203 missense variant G/A;C snv 8.0E-06 2
rs34289250
BRIP1
0.925 0.120 17 61803285 intron variant T/C snv 7.8E-03 2
rs367899983
BNC2
1.000 0.120 9 16864524 intron variant GTCT/- delins 4.2E-05 2
rs10756819
BNC2
1.000 0.120 9 16858086 intron variant G/A;C;T snv 1
rs10810666 1.000 0.120 9 16911668 intergenic variant C/T snv 0.14 1
rs10962656 1.000 0.120 9 16877790 intergenic variant G/A snv 0.10 1
rs1199923024
BRIP1
1.000 0.120 17 61683945 missense variant G/A snv 1.6E-05 7.0E-06 1
rs121913340
BRAF
1.000 0.120 7 140753379 missense variant C/T snv 1
rs12379183
BNC2
1.000 0.120 9 16865701 intron variant A/G snv 0.26 1
rs12379687
BNC2
1.000 0.120 9 16854369 intron variant G/A;T snv 1
rs12451939
MED13
1.000 0.120 17 61970281 intron variant A/G snv 2.6E-02 1
rs12937080
BRIP1
1.000 0.120 17 61852376 intron variant A/G;T snv 1
rs12938171
INTS2
1.000 0.120 17 61902994 intron variant G/A snv 9.0E-03 1
rs1339552
BNC2
1.000 0.120 9 16848792 intron variant C/T snv 0.52 1