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: rs116315504
rs116315504
1 1.000 0.080 1 203820951 intron variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs12123537
rs12123537
1 1.000 0.080 1 203822046 intron variant C/G;T snv 0.700 1.000 1 2017 2017