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: rs1555954154
rs1555954154
1 1.000 X 41346399 missense variant G/A snv 0.700 0
dbSNP: rs797045024
rs797045024
1 1.000 X 41346527 missense variant T/C snv 0.800 0
dbSNP: rs796052226
rs796052226
1 1.000 X 41346548 missense variant T/C snv 0.700 0
dbSNP: rs1555954284
rs1555954284
24 0.752 0.360 X 41346607 missense variant C/T snv 0.700 0
dbSNP: rs1057519430
rs1057519430
5 0.925 X 41346946 missense variant C/T snv 0.800 0
dbSNP: rs886041705
rs886041705
1 1.000 X 41347349 stop gained C/T snv 0.700 0