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: rs7341475
rs7341475
6 0.851 0.240 7 103764368 intron variant G/A snv 0.17 0.860 0.857 7 2008 2019
dbSNP: rs12705169
rs12705169
1 1.000 0.040 7 103936441 intron variant T/C;G snv 0.010 1.000 1 2011 2011
dbSNP: rs262355
rs262355
1 1.000 0.040 7 103785668 intron variant A/T snv 0.67 0.010 1.000 1 2015 2015
dbSNP: rs362719
rs362719
2 0.925 0.040 7 103545430 intron variant C/A snv 0.32 0.010 1.000 1 2011 2011
dbSNP: rs362746
rs362746
2 0.925 0.120 7 103539148 synonymous variant A/G snv 3.8E-02 2.1E-02 0.010 1.000 1 2019 2019
dbSNP: rs362814
rs362814
1 1.000 0.040 7 103574673 intron variant T/A snv 0.75 0.010 1.000 1 2019 2019
dbSNP: rs39339
rs39339
1 1.000 0.040 7 103819488 intron variant T/G snv 0.17 0.010 1.000 1 2019 2019
dbSNP: rs540058
rs540058
1 1.000 0.040 7 103719273 intron variant T/C snv 0.13 0.010 1.000 1 2019 2019
dbSNP: rs661575
rs661575
1 1.000 0.040 7 103757660 intron variant T/A;C snv 0.010 1.000 1 2019 2019
dbSNP: rs736707
rs736707
6 0.851 0.040 7 103489956 intron variant A/G snv 0.30 0.010 1.000 1 2017 2017
dbSNP: rs761198705
rs761198705
1 1.000 0.040 7 103490698 missense variant G/C snv 4.0E-06 0.010 1.000 1 2016 2016