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: rs796052235
rs796052235
1 1.000 X 41346376 missense variant G/A snv 0.800 0
dbSNP: rs797045024
rs797045024
1 1.000 X 41346527 missense variant T/C snv 0.800 0
dbSNP: rs797045026
rs797045026
1 1.000 X 41345238 missense variant C/T snv 0.800 0
dbSNP: rs869312692
rs869312692
2 1.000 X 41343291 stop gained C/T snv 0.700 0
dbSNP: rs869320681
rs869320681
1 1.000 X 41344247 stop gained C/A snv 0.700 0
dbSNP: rs886041705
rs886041705
1 1.000 X 41347349 stop gained C/T snv 0.700 0