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: rs1045241
rs1045241
6 1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 0.700 1.000 3 2015 2019
dbSNP: rs1509141
rs1509141
1 5 119356523 intron variant G/C;T snv 0.700 1.000 1 2019 2019