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: rs1557182692
rs1557182692
EMD
3 0.925 0.120 X 154381106 frameshift variant TCTGG/- del 0.700 1.000 1 1999 1999
dbSNP: rs1057518887
rs1057518887
SEPSECS
7 0.925 0.160 4 25156851 splice region variant C/T snv 0.700 0
dbSNP: rs564856283
rs564856283
MYBPC1
3 12 101642495 missense variant G/A;C snv 3.2E-05 0.700 0