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: rs2282032
rs2282032
1 14 90292547 non coding transcript exon variant G/T snv 0.18 0.800 1.000 1 2010 2010
dbSNP: rs4904670
rs4904670
1 14 90303866 intron variant C/G;T snv 0.700 1.000 1 2015 2015