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: rs11038993
rs11038993
1 11 46789366 intron variant C/A snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs4506602
rs4506602
1 11 46794083 intron variant C/G;T snv 0.700 1.000 1 2013 2013