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: rs1256049
rs1256049
32 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 0.010 1.000 1 2012 2012
dbSNP: rs3020449
rs3020449
10 0.807 0.200 14 64306674 intron variant A/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs3020450
rs3020450
10 0.807 0.200 14 64301584 splice region variant C/A;T snv 0.010 1.000 1 2013 2013
dbSNP: rs4986938
rs4986938
35 0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 0.010 1.000 1 2012 2012