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: rs587777392
rs587777392
1 1.000 1 109630697 missense variant G/C snv 0.800 1.000 1 2013 2013
dbSNP: rs587777394
rs587777394
1 1.000 1 109630740 missense variant G/T snv 0.800 1.000 1 2013 2013
dbSNP: rs587777395
rs587777395
1 1.000 1 109629487 missense variant G/A;T snv 2.0E-05; 4.0E-06 0.800 1.000 1 2013 2013
dbSNP: rs1553230375
rs1553230375
1 1.000 1 109630690 stop lost T/G snv 0.700 0
dbSNP: rs587777391
rs587777391
1 1.000 1 109628725 frameshift variant G/- delins 0.700 0
dbSNP: rs587777393
rs587777393
1 1.000 1 109627453 stop gained C/A snv 4.0E-06 0.700 0
dbSNP: rs875989844
rs875989844
1 1.000 1 109630343 stop gained C/G snv 0.700 0