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: rs539738963
rs539738963
1 1.000 0.080 1 36348807 missense variant C/T snv 2.2E-05 1.4E-05 0.700 0
dbSNP: rs755089893
rs755089893
1 1.000 0.080 1 36355378 missense variant A/G snv 4.0E-06; 8.0E-06 0.700 0