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: rs11591860
rs11591860
1 10 131925501 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs12761761
rs12761761
2 10 131961871 downstream gene variant C/T snv 0.21 0.700 1.000 1 2018 2018