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: rs34684276
rs34684276
3 15 78520813 intron variant G/A snv 0.24 0.700 1.000 1 2015 2015
dbSNP: rs9788721
rs9788721
6 1.000 0.040 15 78510527 intron variant C/T snv 0.65 0.700 1.000 1 2017 2017