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: rs11807350
rs11807350
1 1.000 0.040 1 161191145 missense variant C/T snv 3.1E-04 4.7E-04 0.010 < 0.001 1 2016 2016
dbSNP: rs4233367
rs4233367
2 0.925 0.040 1 161193247 missense variant T/A;C snv 0.67 0.010 < 0.001 1 2016 2016