Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17432750 5 56735995 regulatory region variant C/A snv 0.13 2
rs4912474 3 184148698 upstream gene variant C/A snv 0.35 2
rs6993464 8 119532708 intergenic variant C/A;T snv 2
rs74345699 5 56757652 intergenic variant C/A;T snv 2
rs895919 11 132360808 regulatory region variant T/C snv 0.38 2
rs9257445 6 28981429 upstream gene variant G/C snv 0.34 2
rs1204442125
ADAM17
2 9527876 missense variant G/A snv 2
rs560209396
ADAM9 ; TM2D2
8 38996229 missense variant T/C snv 8.0E-06 2
rs3737482
ADH7
4 99428309 intron variant T/C snv 1.0E-02 2
rs2498794
AKT1
14 104778914 intron variant A/G snv 0.54 2
rs1171303257
ALB
4 73410405 missense variant G/C snv 4.0E-06 2
rs55674018
ALPK2
18 58524007 missense variant G/C snv 5.1E-04 1.1E-04 2
rs3735400
ANLN
7 36399100 missense variant C/G;T snv 0.13 2
rs1322051434
APC
5 112838427 missense variant A/T snv 7.0E-06 2
rs1439772141
APC
5 112837677 missense variant C/G snv 2
rs755105138
APC
5 112837554 missense variant C/A;G snv 4.0E-06 2
rs781561221
APC
5 112792452 missense variant A/G snv 4.0E-06 2
rs1284653043
ATG7
3 11313353 missense variant G/A snv 4.0E-06 7.0E-06 2
rs143125796
ATXN1
6 16327884 missense variant T/C snv 6.1E-05 3.5E-04 2
rs1393141051
BARD1
2 214745749 missense variant T/C snv 2
rs6060627
BCL2L1
20 31674356 intron variant C/T snv 0.41 2
rs750275408
BRCA1
17 43104237 missense variant T/C snv 2
rs786203797
BRCA1
17 43095876 missense variant C/A;T snv 2
rs80357357
BRCA1
17 43104165 missense variant C/T snv 8.0E-06 2.8E-05 2
rs1060502495
BRCA2
13 32332560 missense variant A/G snv 2