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: rs110419
rs110419
8 0.827 0.200 11 8231306 intron variant A/G snv 0.42 0.850 1.000 7 2011 2020
dbSNP: rs2168101
rs2168101
7 0.827 0.200 11 8233861 intron variant C/A snv 0.24 0.730 1.000 4 2017 2020
dbSNP: rs204938
rs204938
3 0.882 0.080 11 8256650 intron variant C/T snv 0.49 0.040 1.000 4 2016 2020
dbSNP: rs110420
rs110420
3 0.882 0.080 11 8231502 intron variant T/C snv 0.42 0.010 1.000 1 2015 2015
dbSNP: rs204926
rs204926
3 0.882 0.080 11 8233559 intron variant G/A snv 0.41 0.010 1.000 1 2015 2015
dbSNP: rs3750952
rs3750952
3 0.882 0.080 11 8230374 synonymous variant G/C;T snv 0.45; 4.8E-05 0.010 1.000 1 2018 2018