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: rs6675281
rs6675281
7 0.827 0.080 1 231818355 missense variant C/T snv 0.11 0.14 0.060 1.000 6 2008 2019
dbSNP: rs1238276682
rs1238276682
1 1.000 0.040 1 231818424 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2007 2007