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: rs4488809
rs4488809
2 0.827 0.080 3 189638472 intron variant T/C snv 0.45 0.750 1.000 3 2011 2019
dbSNP: rs13080835
rs13080835
2 0.925 0.080 3 189639410 intron variant G/T snv 0.45 0.700 1.000 1 2017 2017