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: rs2458413
rs2458413
2 0.925 0.080 8 104347204 intron variant C/T snv 0.44 0.820 0.667 3 2010 2019
dbSNP: rs62620995
rs62620995
1 1.000 0.040 8 104355036 missense variant C/T snv 8.7E-03 9.3E-03 0.010 1.000 1 2017 2017