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: rs1879529
rs1879529
3 15 88871064 intron variant G/T snv 0.28 0.700 1.000 1 2017 2017
dbSNP: rs3817428
rs3817428
3 15 88872016 missense variant C/G snv 0.20 0.20 0.700 1.000 1 2017 2017