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: rs3217978
rs3217978
1 1.000 0.040 9 22007331 intron variant C/A snv 1.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs3217992
rs3217992
22 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 0.700 1.000 1 2014 2014
dbSNP: rs3217989
rs3217989
1 1.000 0.040 9 22003791 3 prime UTR variant T/C snv 7.3E-02 0.010 1.000 1 2011 2011