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: rs1562853011
rs1562853011
SGCE ; CASD1
1 1.000 0.040 7 94623345 inframe insertion -/TATCAAATT delins 0.700 0
dbSNP: rs863223283
rs863223283
SGCE ; CASD1
1 1.000 0.040 7 94600844 frameshift variant GTTTT/- delins 0.700 0
dbSNP: rs863223284
rs863223284
SGCE ; CASD1
1 1.000 0.040 7 94600798 frameshift variant -/A delins 0.700 0
dbSNP: rs863223285
rs863223285
SGCE ; CASD1
1 1.000 0.040 7 94618800 frameshift variant CT/- del 0.700 0