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: rs10754558
rs10754558
20 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 0.030 1.000 3 2014 2018
dbSNP: rs10925019
rs10925019
2 0.925 0.040 1 247432548 intron variant C/T snv 0.11 0.010 1.000 1 2014 2014
dbSNP: rs4925648
rs4925648
2 0.925 0.040 1 247417266 intron variant C/T snv 0.12 0.010 1.000 1 2014 2014