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: rs1553846331
rs1553846331
4 0.925 0.120 4 3473504 missense variant C/T snv 0.700 0
dbSNP: rs756015202
rs756015202
4 0.925 0.120 4 3493047 missense variant C/T snv 5.5E-06 0.700 0