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: rs6761637
rs6761637
1 1.000 0.080 2 118981487 missense variant T/C snv 8.3E-02 0.13 0.020 1.000 2 2011 2018
dbSNP: rs12998782
rs12998782
3 0.882 0.160 2 118967804 intron variant C/T snv 0.19 0.010 1.000 1 2017 2017
dbSNP: rs1371562
rs1371562
1 1.000 0.080 2 118975372 intron variant G/T snv 0.33 0.010 1.000 1 2011 2011
dbSNP: rs17009726
rs17009726
1 1.000 0.080 2 118967884 intron variant A/G snv 1.0E-02 0.010 1.000 1 2011 2011
dbSNP: rs17795618
rs17795618
1 1.000 0.080 2 118973892 intron variant T/A snv 0.12 0.010 1.000 1 2011 2011
dbSNP: rs2011839
rs2011839
1 1.000 0.080 2 118985008 intron variant C/A;T snv 0.010 1.000 1 2011 2011
dbSNP: rs2278589
rs2278589
1 1.000 0.080 2 118971300 intron variant G/A;C snv 0.010 1.000 1 2016 2016
dbSNP: rs6751745
rs6751745
2 0.925 0.080 2 118983428 intron variant C/T snv 0.31 0.010 1.000 1 2016 2016