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: rs13376333
rs13376333
2 0.925 0.080 1 154841877 intron variant C/T snv 0.28 0.870 1.000 7 2010 2015
dbSNP: rs6666258
rs6666258
3 0.882 0.080 1 154841792 intron variant G/C snv 0.30 0.800 1.000 1 2012 2012
dbSNP: rs4999127
rs4999127
1 1.000 0.080 1 154741530 intron variant G/A snv 0.89 0.700 1.000 2 2018 2018
dbSNP: rs34245846
rs34245846
1 1.000 0.080 1 154858667 intron variant A/G snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs34292822
rs34292822
1 1.000 0.080 1 154839924 intron variant G/C snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs36004974
rs36004974
1 1.000 0.080 1 154845927 intron variant A/G snv 0.25 0.700 1.000 1 2017 2017
dbSNP: rs1131820
rs1131820
2 0.925 0.080 1 154772376 synonymous variant A/G snv 0.77 0.71 0.020 1.000 2 2011 2014