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: rs416258
rs416258
3 11 16890089 intron variant G/C snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs448671
rs448671
2 11 16878556 intron variant T/G snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs7940807
rs7940807
2 11 16892459 intron variant G/T snv 0.21 0.700 1.000 1 2018 2018