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: rs3006802
rs3006802
2 10 26447311 intron variant T/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs7098710
rs7098710
1 10 26446058 intron variant C/T snv 0.32 0.700 1.000 1 2019 2019