Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs4849887 0.807 0.080 2 120487546 intergenic variant T/A;C snv 7
rs4415084 0.827 0.080 5 44662413 upstream gene variant C/T snv 0.49 6
rs10771399 0.827 0.080 12 28002147 intergenic variant A/G snv 8.9E-02 5
rs718282 0.925 0.080 7 152638744 intergenic variant A/G snv 0.94 2
rs2363956
ANKLE1
0.776 0.160 19 17283315 missense variant T/G snv 0.48 0.50 8
rs527616
AQP4-AS1
0.851 0.080 18 26757460 intron variant C/G snv 0.71 4
rs1436904
AQP4-AS1 ; CHST9
0.851 0.080 18 26990703 intron variant T/G snv 0.35 4
rs473543
ATG5
0.925 0.080 6 106327811 upstream gene variant A/C;G snv 2
rs8170
BABAM1 ; USHBP1
0.724 0.160 19 17278895 synonymous variant G/A snv 0.15 0.18 13
rs7250266
BABAM1 ; USHBP1
0.925 0.080 19 17266803 intron variant C/G snv 8.5E-02 2
rs587780021
BARD1
0.851 0.200 2 214745842 stop gained G/A snv 2.4E-05 2.8E-05 6
rs587781948
BARD1
0.882 0.200 2 214730491 stop gained G/A snv 1.6E-05 3.5E-05 5
rs799917
BRCA1
0.708 0.320 17 43092919 missense variant G/A;C;T snv 0.40; 1.6E-05 18
rs80356898
BRCA1
0.752 0.200 17 43093844 stop gained G/A;C snv 2.8E-05; 4.0E-06 11
rs8176318
BRCA1
0.807 0.120 17 43045257 3 prime UTR variant C/A snv 0.34 0.29 6
rs80357367
BRCA1
0.851 0.200 17 43057090 stop gained G/A snv 5
rs4986850
BRCA1
0.851 0.080 17 43093454 missense variant C/A;T snv 5.8E-02 4
rs1064793309
BRCA1
0.925 0.080 17 43063889 missense variant C/T snv 2
rs772885662
BRCA1
0.925 0.080 17 43063911 synonymous variant T/C;G snv 4.0E-06; 4.0E-06 2
rs397507758
BRCA2
0.807 0.200 13 32339456 stop gained C/T snv 6
rs552752779
BRIP1
0.925 0.080 17 61784427 splice region variant A/C;G snv 4.0E-06; 2.1E-04 2
rs1651654
C16orf87
0.925 0.080 16 46822677 intron variant T/C snv 0.79 2
rs2814778
CADM3-AS1 ; ACKR1
0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 24
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22