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: rs11471957
rs11471957
2 20 59023277 intron variant -/AA ins 0.700 1.000 1 2016 2016
dbSNP: rs41303899
rs41303899
3 20 59023753 missense variant G/A snv 8.7E-04 9.0E-04 0.700 1.000 1 2016 2016