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 2019 2019
dbSNP: rs1800796
rs1800796
74 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.010 1.000 1 2017 2017
dbSNP: rs2069825
rs2069825
2 1.000 0.040 7 22725718 non coding transcript exon variant -/CC delins 6.7E-05 0.010 1.000 1 2011 2011
dbSNP: rs2069840
rs2069840
13 0.742 0.360 7 22728953 intron variant C/G snv 0.27 0.010 1.000 1 2008 2008