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: rs1568362252
rs1568362252
1 19 15192490 missense variant C/T snv 0.700 0
dbSNP: rs28933696
rs28933696
3 0.882 0.160 19 15192134 missense variant G/A snv 0.700 0