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: rs193922626
rs193922626
1 1 237590901 missense variant G/A;C snv 1.6E-05; 4.8E-05 0.700 0
dbSNP: rs794728826
rs794728826
1 1 237781618 missense variant G/A snv 0.700 0