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: rs10830963
rs10830963
27 0.776 0.400 11 92975544 intron variant C/G snv 0.22 0.010 1.000 1 2018 2018
dbSNP: rs8192552
rs8192552
2 1.000 0.080 11 92969796 missense variant G/A snv 6.8E-02 7.4E-02 0.010 1.000 1 2018 2018