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: rs1560465785
rs1560465785
1 1.000 0.080 4 41746307 missense variant G/C snv 0.700 0
dbSNP: rs28647582
rs28647582
3 0.882 0.200 4 41747248 intron variant T/C snv 0.38 0.010 1.000 1 2019 2019