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: rs10766533
rs10766533
4 11 19203130 intron variant T/A snv 0.62 0.700 1.000 1 2016 2016
dbSNP: rs77055095
rs77055095
2 11 19199971 intron variant G/A snv 0.22 0.700 1.000 1 2019 2019