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: rs660895
rs660895
10 0.752 0.360 6 32609603 intergenic variant A/G snv 0.19 0.810 1.000 4 2007 2018
dbSNP: rs615672
rs615672
6 0.851 0.240 6 32606394 intergenic variant G/A;C snv 0.800 1.000 2 2007 2011
dbSNP: rs2516049
rs2516049
12 0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 0.700 1.000 4 2007 2011
dbSNP: rs9270657
rs9270657
2 0.925 0.160 6 32598244 intergenic variant T/G snv 0.42 0.700 1.000 1 2011 2011
dbSNP: rs17879469
rs17879469
9 0.763 0.360 6 32584333 missense variant C/G snv 1.3E-05 0.020 1.000 2 1998 1999
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