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: rs9507287
rs9507287
5 0.851 0.040 13 24212439 intron variant T/C snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs9511143
rs9511143
1 1.000 0.040 13 24200509 intron variant C/T snv 0.56 0.700 1.000 1 2016 2016