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: rs143683481
rs143683481
1 1.000 0.080 2 26278736 missense variant G/A snv 9.1E-05 3.1E-04 0.010 1.000 1 2019 2019
dbSNP: rs750956714
rs750956714
1 1.000 0.080 2 26277125 missense variant T/C snv 4.0E-06 0.010 1.000 1 2019 2019