Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs104886122
rs104886122
COL4A5
1 1.000 0.160 X 108597043 missense variant G/A snv 0.700 0
dbSNP: rs104886124
rs104886124
COL4A5
1 1.000 0.160 X 108597069 splice donor variant G/- del 0.700 0
dbSNP: rs104886125
rs104886125
COL4A5
1 1.000 0.160 X 108597396 missense variant G/A snv 0.700 0
dbSNP: rs104886126
rs104886126
COL4A5
2 0.925 0.160 X 108597422 missense variant G/C snv 0.700 0
dbSNP: rs104886127
rs104886127
COL4A5
2 0.925 0.160 X 108597423 missense variant G/T snv 0.700 0
dbSNP: rs104886128
rs104886128
COL4A5
1 1.000 0.160 X 108597442 frameshift variant C/- del 0.700 0
dbSNP: rs104886129
rs104886129
COL4A5
2 0.925 0.160 X 108597461 missense variant G/C snv 0.700 0
dbSNP: rs104886130
rs104886130
COL4A5
2 0.925 0.160 X 108597525 missense variant G/A snv 0.700 0
dbSNP: rs104886133
rs104886133
COL4A5
2 0.925 0.160 X 108598730 missense variant G/T snv 0.700 0
dbSNP: rs104886134
rs104886134
COL4A5
2 0.925 0.160 X 108598835 missense variant G/A;C;T snv 0.700 0
dbSNP: rs104886135
rs104886135
COL4A5
2 0.925 0.160 X 108598747 missense variant G/C snv 0.700 0
dbSNP: rs104886136
rs104886136
COL4A5
2 0.925 0.160 X 108597470 missense variant G/A snv 0.700 0
dbSNP: rs104886137
rs104886137
COL4A5
2 0.925 0.160 X 108597489 missense variant G/C snv 0.700 0
dbSNP: rs104886138
rs104886138
COL4A5
2 0.925 0.160 X 108597507 missense variant G/A snv 0.700 0
dbSNP: rs104886139
rs104886139
COL4A5
2 0.925 0.160 X 108597524 missense variant G/A snv 0.700 0
dbSNP: rs104886140
rs104886140
COL4A5
2 0.925 0.160 X 108598748 missense variant G/A;T snv 0.700 0
dbSNP: rs104886141
rs104886141
COL4A5
2 0.925 0.160 X 108598783 missense variant G/A;T snv 0.700 0
dbSNP: rs104886144
rs104886144
COL4A5
2 0.925 0.160 X 108598808 missense variant G/A snv 0.700 0
dbSNP: rs104886145
rs104886145
COL4A5
2 0.925 0.160 X 108598817 missense variant G/A snv 0.700 0
dbSNP: rs104886147
rs104886147
COL4A5
2 0.925 0.160 X 108598834 missense variant G/A snv 0.700 0
dbSNP: rs104886150
rs104886150
COL4A5
2 0.925 0.160 X 108601401 missense variant G/A snv 0.700 0
dbSNP: rs104886151
rs104886151
COL4A5
2 0.925 0.160 X 108601450 missense variant G/C snv 0.700 0
dbSNP: rs104886152
rs104886152
COL4A5
1 1.000 0.160 X 108601401 frameshift variant G/- delins 0.700 0
dbSNP: rs104886153
rs104886153
COL4A5
1 1.000 0.160 X 108601441 missense variant G/A;T snv 0.700 0
dbSNP: rs104886156
rs104886156
COL4A5
1 1.000 0.160 X 108601462 frameshift variant G/- del 0.700 0