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: rs4500751
rs4500751
1 16 15046354 intron variant C/T snv 0.30 0.800 1.000 1 2012 2012
dbSNP: rs4985167
rs4985167
1 16 14989008 non coding transcript exon variant C/T snv 0.25 0.700 1.000 1 2011 2011
dbSNP: rs7200543
rs7200543
6 16 15036113 synonymous variant A/G snv 0.35 0.30 0.700 1.000 1 2011 2011