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: rs1560184664
rs1560184664
CC2D2A
3 0.882 0.360 4 15563461 frameshift variant TA/- delins 0.700 0
dbSNP: rs202149403
rs202149403
TMEM67
4 0.851 0.360 8 93780633 missense variant T/C;G snv 8.4E-05 0.700 0
dbSNP: rs370880399
rs370880399
CC2D2A
5 0.827 0.360 4 15563395 stop gained C/T snv 1.0E-04 1.0E-04 0.700 0
dbSNP: rs386833750
rs386833750
CC2D2A
6 0.807 0.360 4 15563485 stop gained C/A;G;T snv 2.0E-05; 2.0E-05 0.700 0
dbSNP: rs758948621
rs758948621
TMEM67
2 0.925 0.280 8 93797329 splice acceptor variant A/C snv 4.0E-06 0.700 0
dbSNP: rs764719093
rs764719093
CC2D2A
3 0.882 0.360 4 15557361 stop gained C/A;T snv 4.0E-06; 4.0E-06; 4.0E-06 0.700 0
dbSNP: rs781252161
rs781252161
CC2D2A
5 0.827 0.360 4 15533284 stop gained C/T snv 1.8E-05 7.0E-06 0.700 0
dbSNP: rs786200867
rs786200867
TMEM67
2 0.925 0.280 8 93808957 splice donor variant G/T snv 0.700 0
dbSNP: rs786200868
rs786200868
TMEM67
1 1.000 0.200 8 93755871 splice region variant G/A snv 7.1E-06 0.700 0
dbSNP: rs863225231
rs863225231
TMEM67
2 0.925 0.280 8 93782455 missense variant C/G snv 7.0E-06 0.700 0
dbSNP: rs863225232
rs863225232
TMEM67
2 0.925 0.280 8 93782402 missense variant C/T snv 7.0E-06 0.700 0
dbSNP: rs863225233
rs863225233
TMEM67
2 0.925 0.280 8 93815365 missense variant T/G snv 0.700 0
dbSNP: rs863225234
rs863225234
TMEM67
2 0.925 0.280 8 93808922 missense variant A/C snv 0.700 0