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: rs9271100
rs9271100
2 0.925 0.120 6 32608701 regulatory region variant T/A;C snv 0.800 1.000 2 2009 2013
dbSNP: rs9270984
rs9270984
1 1.000 0.080 6 32606214 intergenic variant T/A;G snv 0.800 1.000 1 2013 2013
dbSNP: rs660895
rs660895
10 0.752 0.360 6 32609603 intergenic variant A/G snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs9271055
rs9271055
1 1.000 0.080 6 32607592 intergenic variant G/T snv 0.84 0.700 1.000 1 2013 2013
dbSNP: rs16822805
rs16822805
1 1.000 0.080 6 32584172 missense variant C/A;G;T snv 6.1E-04; 7.6E-03 0.010 1.000 1 2000 2000
dbSNP: rs17886882
rs17886882
1 1.000 0.080 6 32584171 missense variant G/A;C;T snv 9.0E-04; 0.12 0.010 1.000 1 2000 2000
dbSNP: rs771131230
rs771131230
2 0.925 0.120 6 32581827 missense variant C/A;T snv 0.010 1.000 1 2011 2011
dbSNP: rs773389640
rs773389640
2 0.925 0.120 6 32581821 missense variant C/G;T snv 0.010 1.000 1 2011 2011