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: rs10798
rs10798
1 11 2848935 3 prime UTR variant A/G snv 0.44 0.38 0.010 1.000 1 2016 2016
dbSNP: rs12720459
rs12720459
7 0.807 0.160 11 2583535 missense variant C/A;G;T snv 0.010 1.000 1 2014 2014
dbSNP: rs199472678
rs199472678
3 0.925 0.120 11 2445430 missense variant A/G snv 8.9E-06 0.010 1.000 1 2009 2009
dbSNP: rs199472742
rs199472742
2 1.000 0.120 11 2572982 missense variant G/T snv 0.010 1.000 1 2002 2002
dbSNP: rs2074238
rs2074238
3 1.000 0.120 11 2463573 intron variant T/A;C snv 0.010 1.000 1 2013 2013
dbSNP: rs8234
rs8234
1 11 2848878 3 prime UTR variant A/G snv 0.45 0.38 0.010 1.000 1 2016 2016