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: rs2075291
rs2075291
4 0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 0.720 1.000 1 2017 2019
dbSNP: rs651821
rs651821
10 0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 0.710 1.000 1 2018 2018