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: rs11696845
rs11696845
1 20 44742679 intron variant C/T snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs6073535
rs6073535
1 20 44745218 intron variant T/C snv 0.37 0.700 1.000 1 2012 2012