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: rs210134
rs210134
3 1.000 0.120 6 33572432 intron variant A/G snv 0.72 0.800 1.000 6 2011 2019
dbSNP: rs513349
rs513349
2 1.000 0.120 6 33573942 intron variant A/G snv 0.51 0.51 0.800 1.000 2 2013 2019
dbSNP: rs5745568
rs5745568
4 0.882 0.080 6 33580617 intron variant G/T snv 0.19 0.700 1.000 3 2010 2019
dbSNP: rs9296095
rs9296095
1 6 33574746 intron variant T/C snv 0.25 0.700 1.000 2 2014 2019
dbSNP: rs210135
rs210135
1 6 33572915 3 prime UTR variant T/A;C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs210142
rs210142
3 0.925 0.120 6 33579060 intron variant T/C snv 0.74 0.700 1.000 1 2016 2016
dbSNP: rs210143
rs210143
6 0.827 0.160 6 33579153 intron variant T/C snv 0.74 0.700 1.000 1 2018 2018