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: rs139860229
rs139860229
1 1.000 0.080 17 10497766 missense variant C/T snv 5.6E-05 8.4E-05 0.700 0
dbSNP: rs150456818
rs150456818
1 1.000 0.080 17 10496414 missense variant C/T snv 8.4E-05 2.9E-04 0.700 0
dbSNP: rs752643679
rs752643679
1 1.000 0.080 17 10499041 missense variant G/A snv 3.6E-05 2.1E-05 0.700 0