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: rs1044032
rs1044032
2 0.925 0.080 15 45676237 missense variant T/C snv 0.24 0.19 0.020 1.000 2 2015 2018