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: rs10994359
rs10994359
7 0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 0.810 1.000 3 2011 2014
dbSNP: rs16915157
rs16915157
1 1.000 0.040 10 60586880 intron variant C/T snv 0.19 0.800 1.000 1 2012 2012
dbSNP: rs10994397
rs10994397
5 0.851 0.040 10 60519366 intron variant C/T snv 9.5E-02 0.700 1.000 1 2013 2013
dbSNP: rs10761482
rs10761482
4 0.851 0.120 10 60325579 intron variant T/C snv 0.70 0.040 0.750 4 2010 2014
dbSNP: rs10994336
rs10994336
12 0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 0.040 1.000 4 2011 2016
dbSNP: rs41283526
rs41283526
2 0.925 0.040 10 60145969 splice region variant T/C snv 7.6E-03 8.2E-03 0.020 1.000 2 2016 2018
dbSNP: rs10994338
rs10994338
3 0.882 0.040 10 60421370 intron variant G/A snv 7.5E-02 0.010 1.000 1 2016 2016
dbSNP: rs3808942
rs3808942
1 1.000 0.040 10 60391090 intron variant C/T snv 0.73 0.010 1.000 1 2012 2012
dbSNP: rs3808943
rs3808943
2 0.925 0.040 10 60391257 intron variant C/T snv 9.7E-02 0.010 1.000 1 2012 2012
dbSNP: rs4948418
rs4948418
2 0.925 0.040 10 60425736 intron variant C/T snv 7.9E-02 0.010 1.000 1 2016 2016
dbSNP: rs958852
rs958852
1 1.000 0.040 10 60562860 intron variant T/A snv 0.67 0.010 1.000 1 2016 2016
dbSNP: rs9804190
rs9804190
5 0.882 0.040 10 60080073 intron variant C/T snv 0.30 0.010 1.000 1 2012 2012