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: rs36053993
rs36053993
9 0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 0.700 1.000 23 2002 2014
dbSNP: rs121908382
rs121908382
2 1.000 0.080 1 45331530 missense variant G/A snv 0.700 0
dbSNP: rs121908383
rs121908383
2 1.000 0.080 1 45331502 missense variant T/C snv 0.700 0
dbSNP: rs140342925
rs140342925
5 0.882 0.120 1 45332445 missense variant C/T snv 8.4E-05 8.4E-05 0.700 0
dbSNP: rs1553125914
rs1553125914
2 1.000 0.120 1 45331512 frameshift variant -/TC delins 0.700 0
dbSNP: rs34612342
rs34612342
11 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.700 0
dbSNP: rs372267274
rs372267274
5 0.882 0.120 1 45333171 splice acceptor variant C/G;T snv 0.700 0
dbSNP: rs587780088
rs587780088
5 0.882 0.120 1 45334493 stop gained G/A;C snv 8.0E-06; 4.0E-06 0.700 0
dbSNP: rs587781628
rs587781628
5 0.882 0.120 1 45331558 splice acceptor variant T/C snv 2.4E-05 7.0E-06 0.700 0