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: rs4794820
rs4794820
9 0.790 0.160 17 39933091 intron variant A/G;T snv 0.700 1.000 1 2007 2007
dbSNP: rs4795405
rs4795405
6 0.851 0.160 17 39932164 intron variant T/A;C snv 0.700 1.000 1 2007 2007
dbSNP: rs6503525
rs6503525
2 0.925 0.080 17 39938921 intron variant G/A;C snv 0.700 1.000 1 2007 2007
dbSNP: rs8065126
rs8065126
2 1.000 0.080 17 39942782 intron variant T/A;C snv 0.700 1.000 1 2007 2007
dbSNP: rs8079416
rs8079416
2 0.925 0.080 17 39936460 intron variant T/C snv 0.45 0.700 1.000 1 2007 2007
dbSNP: rs12603332
rs12603332
7 0.807 0.200 17 39926554 5 prime UTR variant T/C snv 0.49 0.010 1.000 1 2019 2019