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: rs758900778
rs758900778
2 0.925 0.080 1 45333489 missense variant G/C snv 4.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs79777494
rs79777494
2 0.882 0.120 1 45334495 missense variant G/A snv 1.1E-03 4.9E-04 0.010 1.000 1 2008 2008