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: rs857684
rs857684
2 1 158605939 intron variant C/T snv 0.24 0.800 1.000 2 2012 2017
dbSNP: rs12128171
rs12128171
1 1 158610687 3 prime UTR variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2479868
rs2479868
2 1 158610279 3 prime UTR variant C/T snv 0.26 0.700 1.000 1 2012 2012
dbSNP: rs857685
rs857685
1 1 158607319 missense variant A/C;G;T snv 0.27; 4.0E-06; 4.0E-06 0.700 1.000 1 2012 2012
dbSNP: rs857686
rs857686
1 1 158607998 3 prime UTR variant C/A snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs857688
rs857688
1 1 158608228 3 prime UTR variant T/C snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs860772
rs860772
1 1 158606310 intron variant G/C snv 0.23 0.700 1.000 1 2012 2012