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: rs2297067
rs2297067
2 1.000 0.080 14 103100448 missense variant C/T snv 0.22 0.20 0.800 1.000 1 2011 2015
dbSNP: rs8017161
rs8017161
1 0.925 0.080 14 103096858 intron variant G/A snv 0.38 0.800 1.000 1 2011 2011