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: rs6718655
rs6718655
1 2 241556432 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs6733504
rs6733504
2 2 241556538 intron variant A/G;T snv 0.700 1.000 1 2019 2019