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: rs3738401
rs3738401
4 0.882 0.080 1 231694549 missense variant G/A snv 0.30 0.26 0.010 1.000 1 2007 2007
dbSNP: rs751229
rs751229
2 1.000 0.040 1 231632793 intron variant A/G;T snv 0.010 1.000 1 2007 2007