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: rs3760138
rs3760138
6 0.807 0.160 17 76467027 intron variant G/A;T snv 0.010 1.000 1 2010 2010
dbSNP: rs4238989
rs4238989
4 0.851 0.120 17 76467306 intron variant C/G snv 0.45 0.010 1.000 1 2010 2010
dbSNP: rs8150
rs8150
6 0.807 0.160 17 76470935 3 prime UTR variant G/A;C snv 0.010 1.000 1 2010 2010