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: rs3731863
rs3731863
2 0.925 0.040 2 218387485 intron variant C/T snv 8.0E-02 0.010 1.000 1 2009 2009
dbSNP: rs3731865
rs3731865
5 0.882 0.160 2 218385280 non coding transcript exon variant G/A;C;T snv 0.23; 1.4E-04 0.010 1.000 1 2009 2009