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: rs9285583
rs9285583
1 14 54964717 intron variant T/C snv 0.43 0.700 1.000 1 2012 2012
dbSNP: rs943914
rs943914
1 14 54973350 intron variant C/A snv 0.34 0.700 1.000 1 2012 2012