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: rs11602954
rs11602954
2 11 202856 intron variant G/A snv 0.17 0.800 1.000 2 2009 2012
dbSNP: rs11604127
rs11604127
2 11 196944 5 prime UTR variant C/T snv 0.17 0.700 1.000 1 2016 2016
dbSNP: rs2294081
rs2294081
1 11 193863 stop gained T/A;C snv 0.700 1.000 1 2016 2016