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: rs1553354952
rs1553354952
4 0.882 0.200 1 224404492 missense variant C/T snv 0.700 0
dbSNP: rs1553354956
rs1553354956
4 0.882 0.200 1 224404504 missense variant A/C snv 0.700 0