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: rs886042098
rs886042098
IVD
1 1.000 0.080 15 40414967 missense variant C/T snv 0.700 0
dbSNP: rs907414760
rs907414760
IVD
1 1.000 0.080 15 40405871 stop gained G/A;C snv 7.0E-06 0.700 0
dbSNP: rs928991928
rs928991928
IVD
1 1.000 0.080 15 40405972 splice donor variant G/A;C snv 0.700 0
dbSNP: rs982218848
rs982218848
IVD
1 1.000 0.080 15 40418166 missense variant G/A snv 1.2E-05 2.1E-05 0.700 0
dbSNP: rs1267969615
rs1267969615
ACE
100 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.010 1.000 1 2010 2010