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: rs3863150
rs3863150
1 1.000 0.120 5 41506758 intron variant T/C snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs676328
rs676328
1 1.000 0.120 5 41505587 intron variant T/A;C snv 0.700 1.000 1 2012 2012