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: rs3813356
rs3813356
2 6 132513379 upstream gene variant C/T snv 0.37 0.700 1.000 2 2017 2019
dbSNP: rs9493341
rs9493341
2 6 132509805 intron variant A/G snv 0.34 0.700 1.000 1 2016 2016