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: rs1765174
rs1765174
1 10 34279104 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs641162
rs641162
1 10 34277992 intron variant G/A;T snv 0.700 1.000 1 2018 2018