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: rs1501299
rs1501299
52 0.597 0.720 3 186853334 intron variant G/C;T snv 0.020 1.000 2 2011 2013
dbSNP: rs182052
rs182052
18 0.701 0.440 3 186842993 intron variant G/A snv 0.38 0.010 < 0.001 1 2015 2015
dbSNP: rs2082940
rs2082940
10 0.763 0.480 3 186856375 3 prime UTR variant T/A;C snv 0.010 < 0.001 1 2011 2011
dbSNP: rs2241766
rs2241766
48 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 0.010 1.000 1 2016 2016
dbSNP: rs266729
rs266729
37 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.010 < 0.001 1 2015 2015
dbSNP: rs3774262
rs3774262
5 0.851 0.200 3 186854025 intron variant G/A snv 0.10 0.010 1.000 1 2015 2015
dbSNP: rs822391
rs822391
4 0.925 0.080 3 186846014 intron variant C/T snv 0.85 0.010 < 0.001 1 2011 2011
dbSNP: rs822395
rs822395
10 0.776 0.240 3 186849018 intron variant C/A;G snv 0.010 1.000 1 2013 2013
dbSNP: rs822396
rs822396
16 0.732 0.400 3 186849088 intron variant G/A snv 0.81 0.010 1.000 1 2013 2013