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: rs28904921
rs28904921
12 0.763 0.320 11 108329202 missense variant T/G snv 4.0E-05 6.3E-05 0.700 0
dbSNP: rs587781837
rs587781837
3 1.000 0.200 11 108343348 frameshift variant T/- delins 0.700 0
dbSNP: rs786203008
rs786203008
3 1.000 0.200 11 108317401 frameshift variant T/- delins 0.700 0