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: rs613872
rs613872
6 0.851 0.120 18 55543071 intron variant G/T snv 0.88 0.800 1.000 15 2010 2019
dbSNP: rs1348047
rs1348047
1 1.000 0.080 18 55382827 intron variant G/T snv 0.26 0.020 1.000 2 2019 2019
dbSNP: rs1452787
rs1452787
5 0.827 0.160 18 55539976 intron variant A/G snv 0.24 0.010 1.000 1 2019 2019
dbSNP: rs17089887
rs17089887
1 1.000 0.080 18 55541025 intron variant T/C snv 6.9E-02 0.010 1.000 1 2014 2014
dbSNP: rs784257
rs784257
4 1.000 0.080 18 55729968 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs1799782
rs1799782
151 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.010 1.000 1 2015 2015
dbSNP: rs25487
rs25487
205 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2015 2015