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: rs9479118
rs9479118
2 0.925 0.080 6 151797989 intron variant T/C snv 1.6E-02 0.010 1.000 1 2016 2016
dbSNP: rs9383938
rs9383938
5 0.827 0.160 6 151666222 intron variant G/T snv 0.11 0.720 1.000 3 2011 2014
dbSNP: rs9340799
rs9340799
62 0.583 0.680 6 151842246 intron variant A/G snv 0.32 0.070 0.857 7 2007 2020
dbSNP: rs926778
rs926778
2 0.925 0.080 6 152034647 intron variant C/A snv 0.40 0.010 1.000 1 2015 2015
dbSNP: rs796065354
rs796065354
9 0.882 0.080 6 151944320 missense variant A/G snv 0.760 1.000 9 2000 2013
dbSNP: rs7766585
rs7766585
2 0.925 0.080 6 152074901 intron variant T/A;G snv 0.010 1.000 1 2011 2011
dbSNP: rs767863538
rs767863538
3 0.925 0.080 6 151808207 missense variant C/G;T snv 5.6E-06; 5.6E-06 0.010 1.000 1 2009 2009
dbSNP: rs762292600
rs762292600
7 0.925 0.080 6 151944316 missense variant A/G snv 4.0E-06 1.4E-05 0.020 1.000 2 2016 2018
dbSNP: rs761843408
rs761843408
2 0.925 0.080 6 152125285 synonymous variant A/G snv 3.4E-05 2.8E-05 0.010 1.000 1 2009 2009
dbSNP: rs760503206
rs760503206
2 0.925 0.080 6 151807956 missense variant T/C snv 4.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs757200716
rs757200716
5 0.851 0.160 6 151842617 missense variant G/A snv 8.0E-06 0.020 1.000 2 2011 2014
dbSNP: rs747099645
rs747099645
3 0.882 0.120 6 152061061 missense variant C/T snv 1.6E-05 2.8E-05 0.010 1.000 1 2012 2012
dbSNP: rs746432
rs746432
4 0.851 0.120 6 151808173 synonymous variant G/A;C snv 6.6E-02 7.0E-02 0.010 1.000 1 2007 2007
dbSNP: rs523736
rs523736
2 0.925 0.080 6 151802760 intron variant G/A snv 0.62 0.010 1.000 1 2016 2016
dbSNP: rs3798758
rs3798758
3 0.925 0.080 6 152100719 3 prime UTR variant C/A snv 7.4E-02 0.010 1.000 1 2014 2014
dbSNP: rs3798577
rs3798577
16 0.742 0.320 6 152099995 3 prime UTR variant T/C snv 0.45 0.060 1.000 6 2009 2018
dbSNP: rs3778609
rs3778609
2 0.925 0.080 6 151812052 intron variant C/T snv 0.13 0.010 1.000 1 2019 2019
dbSNP: rs3020314
rs3020314
7 0.790 0.280 6 151949537 intron variant C/G;T snv 0.010 1.000 1 2009 2009
dbSNP: rs3003925
rs3003925
2 0.925 0.080 6 151963323 intron variant G/A snv 0.80 0.010 1.000 1 2008 2008
dbSNP: rs2881766
rs2881766
5 0.882 0.120 6 151797984 intron variant T/G snv 0.35 0.030 1.000 3 2015 2019
dbSNP: rs2747648
rs2747648
2 0.925 0.080 6 152101200 3 prime UTR variant C/T snv 0.98 0.010 1.000 1 2012 2012
dbSNP: rs2273206
rs2273206
5 0.851 0.280 6 152061176 intron variant G/T snv 0.17 0.22 0.010 1.000 1 2015 2015
dbSNP: rs2234693
rs2234693
77 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.100 1.000 11 2007 2020
dbSNP: rs2228480
rs2228480
16 0.724 0.360 6 152098960 synonymous variant G/A snv 0.19 0.18 0.060 0.833 6 2010 2016
dbSNP: rs2144025
rs2144025
4 0.925 0.080 6 151986571 intron variant T/A;C snv 0.010 1.000 1 2008 2008