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: rs1561590396
rs1561590396
1 5 146339801 missense variant C/T snv 0.700 0
dbSNP: rs121909057
rs121909057
2 1.000 0.120 5 146340095 missense variant T/C snv 0.020 1.000 2 2008 2009