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: rs1553255354
rs1553255354
2 1.000 1 229431843 missense variant C/G snv 0.700 1.000 9 2001 2015
dbSNP: rs1553255501
rs1553255501
1 1 229432792 missense variant A/C snv 0.700 1.000 9 2001 2015