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: rs5940
rs5940
3 0.882 0.080 2 187466977 missense variant C/T snv 1.3E-02 1.4E-02 0.010 < 0.001 1 2001 2001
dbSNP: rs7586970
rs7586970
2 0.925 0.040 2 187478770 missense variant T/C;G snv 0.29 0.010 1.000 1 2009 2009