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: rs780209390
rs780209390
1 1.000 4 108863327 missense variant C/T snv 1.6E-05 7.0E-06 0.800 0
dbSNP: rs886037741
rs886037741
1 1.000 4 108846165 stop gained C/A snv 0.700 0