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: rs1127354
rs1127354
26 0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 0.010 1.000 1 2009 2009
dbSNP: rs4442975
rs4442975
7 0.827 0.120 2 217056046 intergenic variant G/T snv 0.47 0.010 1.000 1 2019 2019