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: rs28933369
rs28933369
5 0.925 0.080 17 39724744 missense variant G/A snv 0.700 1.000 2 2004 2007
dbSNP: rs1058808
rs1058808
27 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 0.010 1.000 1 2019 2019
dbSNP: rs1801200
rs1801200
7 0.790 0.200 17 39723335 missense variant A/G;T snv 0.010 1.000 1 2011 2011
dbSNP: rs2643194
rs2643194
2 0.925 0.080 17 39696795 5 prime UTR variant C/T snv 0.67 0.010 1.000 1 2019 2019
dbSNP: rs2934971
rs2934971
2 0.925 0.080 17 39698254 intron variant G/T snv 0.66 0.010 1.000 1 2019 2019