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: rs111874856
rs111874856
1 1.000 0.200 18 21028924 missense variant C/T snv 0.010 1.000 1 2014 2014
dbSNP: rs112108028
rs112108028
1 1.000 0.200 18 20959861 missense variant G/A snv 0.010 1.000 1 2014 2014
dbSNP: rs112130712
rs112130712
1 1.000 0.200 18 20967783 missense variant T/C snv 0.010 1.000 1 2014 2014