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: rs353639
rs353639
5 0.851 0.120 11 35162817 intron variant T/G snv 0.32 0.010 1.000 1 2014 2014
dbSNP: rs8193
rs8193
4 0.925 0.080 11 35229771 3 prime UTR variant C/T snv 0.29 0.010 1.000 1 2020 2020