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: rs1057519635
rs1057519635
1 1.000 14 29626508 missense variant C/T snv 0.800 0
dbSNP: rs1057519636
rs1057519636
1 1.000 14 29638705 missense variant A/C snv 0.800 0