Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28904921
C11orf65 ; ATM
0.763 0.320 11 108329202 missense variant T/G snv 4.0E-05 6.3E-05 7
rs121913121
FH
0.851 0.320 1 241513661 missense variant T/G snv 6
rs7907606 0.790 0.120 10 103920874 upstream gene variant T/G snv 0.26 5
rs2363956
ANKLE1
0.776 0.160 19 17283315 missense variant T/G snv 0.48 0.50 4
rs569550
LSP1
0.925 0.080 11 1865838 intron variant T/G snv 0.35 4
rs1353747
PDE4D
0.882 0.080 5 59041654 intron variant T/G snv 6.9E-02 3
rs41293477
BRCA2
0.851 0.200 13 32337513 stop gained T/G snv 7.0E-06 3
rs45446698
CYP3A7-CYP3A51P ; CYP3A7 ; ZSCAN25
0.807 0.120 7 99735325 upstream gene variant T/G snv 2.7E-02 3
rs80358561
BRCA2
0.851 0.200 13 32319323 stop gained T/G snv 3
rs1436904
AQP4-AS1 ; CHST9
0.851 0.080 18 26990703 intron variant T/G snv 0.35 2
rs3757322
CCDC170
1.000 0.080 6 151621059 3 prime UTR variant T/G snv 0.36 2
rs10825036 0.882 0.080 10 53506471 intergenic variant T/G snv 0.21 1
rs1189020
LINC02284
1.000 0.080 14 56410241 intron variant T/G snv 0.93 1
rs1274649
RAD51B
1.000 0.080 14 68207583 intron variant T/G snv 0.17 1
rs1316014
RAD51B
1.000 0.080 14 68232653 intron variant T/G snv 0.18 1
rs13188458 0.882 0.160 5 8127718 intergenic variant T/G snv 0.22 1
rs13230714
TPK1
1.000 0.080 7 144477198 intron variant T/G snv 0.22 1
rs16886113 0.925 0.080 5 56699208 intergenic variant T/G snv 8.3E-02 1
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 1
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1
rs199501877 1.000 0.080 4 48056416 intergenic variant T/G snv 2.6E-04 1
rs2517388
ASH2L
0.925 0.080 8 38120214 intron variant T/G snv 0.24 1
rs2523992
TRIM31-AS1 ; TRIM31
1.000 0.080 6 30107326 intron variant T/G snv 0.11 1
rs2810650 1.000 0.080 1 203938990 intergenic variant T/G snv 0.25 1
rs2822999
NRIP1
1.000 0.080 21 14992435 non coding transcript exon variant T/G snv 0.13 1