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: rs116843064
rs116843064
16 0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 0.700 1.000 7 2014 2019
dbSNP: rs117760119
rs117760119
1 19 8367853 intron variant C/G;T snv 0.700 1.000 1 2019 2019