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: rs10750097
rs10750097
6 1.000 0.040 11 116793324 upstream gene variant G/A;C snv 0.700 1.000 2 2012 2012
dbSNP: rs662799
rs662799
33 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.700 1.000 2 2012 2012
dbSNP: rs12287066
rs12287066
4 11 116791615 synonymous variant G/T snv 7.7E-02 0.10 0.700 1.000 1 2012 2012
dbSNP: rs2072560
rs2072560
5 11 116791110 missense variant T/C snv 0.89 0.94 0.700 1.000 1 2012 2012
dbSNP: rs2266788
rs2266788
19 0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 0.700 1.000 1 2012 2012
dbSNP: rs34003087
rs34003087
3 11 116792880 upstream gene variant C/T snv 4.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs651821
rs651821
17 0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 0.700 1.000 1 2012 2012