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: rs1800591
rs1800591
3 0.882 0.120 4 99574331 intron variant G/T snv 0.26 0.020 1.000 2 2014 2014
dbSNP: rs1057613
rs1057613
1 1.000 0.040 4 99583828 3 prime UTR variant G/A snv 0.60 0.010 1.000 1 2014 2014
dbSNP: rs1412189378
rs1412189378
1 1.000 0.040 4 99583404 missense variant C/A snv 0.010 1.000 1 2009 2009
dbSNP: rs1800804
rs1800804
1 1.000 0.040 4 99574660 intron variant T/C snv 0.26 0.010 1.000 1 2014 2014
dbSNP: rs2306986
rs2306986
1 1.000 0.040 4 99583418 missense variant G/C;T snv 5.9E-02 0.010 1.000 1 2017 2017
dbSNP: rs3805335
rs3805335
1 1.000 0.040 4 99586478 intron variant C/T snv 1.3E-02 0.010 1.000 1 2014 2014
dbSNP: rs3816873
rs3816873
9 0.790 0.200 4 99583507 missense variant T/C snv 0.25 0.26 0.010 1.000 1 2011 2011
dbSNP: rs61733139
rs61733139
1 1.000 0.040 4 99583409 missense variant G/C snv 4.0E-02 4.9E-02 0.010 1.000 1 2011 2011
dbSNP: rs756998920
rs756998920
1 1.000 0.040 4 99581967 missense variant G/A snv 3.4E-04 8.4E-05 0.010 1.000 1 2017 2017
dbSNP: rs781469754
rs781469754
1 1.000 0.040 4 99591691 missense variant A/G snv 4.0E-06 7.0E-06 0.010 1.000 1 2017 2017