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: rs11620731
rs11620731
2 14 70350424 intron variant T/C snv 0.85 0.700 1.000 1 2018 2018
dbSNP: rs8022288
rs8022288
1 14 70380407 intron variant C/T snv 0.87 0.700 1.000 1 2018 2018