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: rs104893878
rs104893878
21 0.732 0.160 4 89835580 missense variant C/G snv 0.060 1.000 6 2003 2018
dbSNP: rs104893877
rs104893877
59 0.614 0.360 4 89828149 missense variant C/T snv 0.050 1.000 5 2003 2018
dbSNP: rs17016074
rs17016074
4 0.851 0.080 4 89726127 3 prime UTR variant G/A snv 4.7E-02 0.010 1.000 1 2009 2009