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: rs33980500
rs33980500
14 0.742 0.200 6 111592059 missense variant C/T snv 8.6E-02 9.7E-02 0.820 1.000 4 2010 2015
dbSNP: rs13190932
rs13190932
1 1.000 0.080 6 111591867 missense variant G/A snv 5.3E-02 5.0E-02 0.710 1.000 2 2010 2019