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: rs2273073
rs2273073
3 0.882 0.120 20 6770235 missense variant T/C;G snv 2.4E-02 0.010 1.000 1 2008 2008
dbSNP: rs235768
rs235768
8 0.807 0.160 20 6778468 missense variant A/G;T snv 0.67 0.010 1.000 1 2006 2006