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: rs1535
rs1535
24 0.752 0.240 11 61830500 intron variant A/G snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs174594
rs174594
14 0.776 0.160 11 61852357 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs4246215
rs4246215
29 0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 0.700 1.000 1 2019 2019