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: rs1410727652
rs1410727652
2 1.000 0.080 6 160348669 missense variant C/T snv 7.0E-06 0.020 1.000 2 2018 2018