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: rs1800896
rs1800896
113 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.020 1.000 2 2014 2017
dbSNP: rs1800795
rs1800795
140 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2014 2014
dbSNP: rs1800872
rs1800872
119 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2014 2014
dbSNP: rs2856838
rs2856838
4 0.851 0.200 2 112782395 intron variant G/A snv 0.37 0.010 1.000 1 2017 2017
dbSNP: rs4461841
rs4461841
2 0.925 0.160 7 80827525 intron variant C/T snv 0.93 0.91 0.010 1.000 1 2017 2017