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: rs8177374
rs8177374
22 0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 0.040 0.750 4 2008 2016
dbSNP: rs7932766
rs7932766
2 0.925 0.080 11 126292967 synonymous variant C/T snv 0.18 0.19 0.010 < 0.001 1 2011 2011
dbSNP: rs8177400
rs8177400
4 0.882 0.160 11 126292695 missense variant G/A;C;T snv 2.8E-03; 1.2E-05 0.010 1.000 1 2011 2011