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: rs6141
rs6141
4 0.925 0.080 3 184372478 3 prime UTR variant C/G;T snv 4.0E-06; 0.56 0.800 1.000 3 2010 2018
dbSNP: rs78565404
rs78565404
1 3 184372454 3 prime UTR variant C/T snv 6.4E-02 0.700 1.000 2 2016 2016
dbSNP: rs34623301
rs34623301
1 3 184375252 intron variant G/A snv 0.31 0.700 1.000 1 2016 2016