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: rs1800795
rs1800795
140 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2012 2012
dbSNP: rs2069827
rs2069827
1 1.000 0.040 7 22725837 non coding transcript exon variant G/C;T snv 0.010 1.000 1 2012 2012
dbSNP: rs2069840
rs2069840
13 0.742 0.360 7 22728953 intron variant C/G snv 0.27 0.010 1.000 1 2012 2012