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: rs104886080
rs104886080
COL4A5
2 0.925 0.160 X 108580983 missense variant G/A snv 0.700 0
dbSNP: rs104886081
rs104886081
COL4A5
1 1.000 0.160 X 108581004 stop gained G/T snv 0.700 0
dbSNP: rs104886083
rs104886083
COL4A5
1 1.000 0.160 X 108581019 missense variant G/A snv 0.700 0
dbSNP: rs104886084
rs104886084
COL4A5
1 1.000 0.160 X 108582884 missense variant G/A snv 0.700 0
dbSNP: rs104886085
rs104886085
COL4A5
2 0.925 0.160 X 108582902 missense variant G/C snv 0.700 0
dbSNP: rs104886086
rs104886086
COL4A5
1 1.000 0.160 X 108582903 missense variant G/A snv 0.700 0
dbSNP: rs104886088
rs104886088
COL4A5
3 0.882 0.160 X 108582920 stop gained G/A;T snv 0.700 0
dbSNP: rs104886092
rs104886092
COL4A5
2 0.925 0.160 X 108584485 missense variant G/T snv 0.700 0
dbSNP: rs104886093
rs104886093
COL4A5
1 1.000 0.160 X 108584494 missense variant G/T snv 0.700 0
dbSNP: rs104886094
rs104886094
COL4A5
1 1.000 0.160 X 108586699 stop gained C/T snv 0.700 0
dbSNP: rs104886096
rs104886096
COL4A5
2 0.925 0.160 X 108586676 missense variant G/A snv 0.700 0
dbSNP: rs104886097
rs104886097
COL4A5
2 0.925 0.160 X 108586694 missense variant G/A snv 0.700 0
dbSNP: rs104886098
rs104886098
COL4A5
1 1.000 0.160 X 108586721 missense variant G/A snv 0.700 0
dbSNP: rs104886099
rs104886099
COL4A5
1 1.000 0.160 X 108591100 missense variant G/T snv 0.700 0
dbSNP: rs104886101
rs104886101
COL4A5
2 0.925 0.160 X 108591118 missense variant G/A snv 0.700 0
dbSNP: rs104886103
rs104886103
COL4A5
2 0.925 0.160 X 108591135 missense variant G/A snv 0.700 0
dbSNP: rs104886105
rs104886105
COL4A5
2 0.925 0.160 X 108586730 missense variant G/A snv 0.700 0
dbSNP: rs104886108
rs104886108
COL4A5
2 0.925 0.160 X 108586703 missense variant G/C snv 0.700 0
dbSNP: rs104886110
rs104886110
COL4A5
2 0.925 0.160 X 108591160 missense variant G/A snv 0.700 0
dbSNP: rs104886111
rs104886111
COL4A5
1 1.000 0.160 X 108591168 missense variant G/A snv 9.4E-06 0.700 0
dbSNP: rs104886112
rs104886112
COL4A5
1 1.000 0.160 X 108591178 missense variant G/A snv 0.700 0
dbSNP: rs104886113
rs104886113
COL4A5
2 0.925 0.160 X 108591592 frameshift variant C/-;CC delins 0.700 0
dbSNP: rs104886114
rs104886114
COL4A5
2 0.925 0.160 X 108591618 missense variant G/A snv 0.700 0
dbSNP: rs104886115
rs104886115
COL4A5
1 1.000 0.160 X 108591627 missense variant G/A snv 0.700 0
dbSNP: rs104886116
rs104886116
COL4A5
3 0.882 0.160 X 108591635 missense variant G/A snv 0.700 0