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: rs472402
rs472402
2 0.925 0.080 5 6635478 intron variant G/C snv 0.53 0.020 1.000 2 2016 2019
dbSNP: rs3822430
rs3822430
2 0.925 0.080 5 6651857 synonymous variant A/G snv 0.33 0.35 0.010 1.000 1 2016 2016