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: rs10838435
rs10838435
2 11 45223352 intron variant C/G snv 0.70 0.700 1.000 1 2019 2019
dbSNP: rs2863171
rs2863171
1 11 45229181 3 prime UTR variant A/C snv 0.21 0.700 1.000 1 2014 2014
dbSNP: rs73464505
rs73464505
1 11 45101435 intron variant A/C;T snv 0.700 1.000 1 2019 2019