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: rs7453920
rs7453920
10 0.752 0.440 6 32762235 intron variant A/G;T snv 0.880 0.909 11 2011 2017
dbSNP: rs7756516
rs7756516
4 0.851 0.280 6 32756140 3 prime UTR variant C/T snv 0.49 0.710 1.000 1 2014 2014
dbSNP: rs2051549
rs2051549
4 0.851 0.280 6 32762309 intron variant G/A snv 0.64 0.700 1.000 1 2013 2013
dbSNP: rs2071551
rs2071551
1 1.000 0.080 6 32761682 synonymous variant C/G;T snv 0.67 0.700 1.000 1 2013 2013
dbSNP: rs2301271
rs2301271
3 0.882 0.240 6 32757416 intron variant A/G snv 0.60 0.700 1.000 1 2011 2011
dbSNP: rs762815
rs762815
1 1.000 0.080 6 32761865 synonymous variant G/A;C snv 4.1E-06; 0.66 0.700 1.000 1 2013 2013
dbSNP: rs7768538
rs7768538
2 0.925 0.160 6 32762044 intron variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs9276583
rs9276583
1 1.000 0.080 6 32762103 intron variant G/A snv 0.63 0.700 1.000 1 2013 2013