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: rs10864315
rs10864315
3 1 7790021 intron variant C/T snv 0.28 0.010 1.000 1 2016 2016
dbSNP: rs2640909
rs2640909
4 1 7830057 missense variant T/C snv 0.14 0.23 0.010 1.000 1 2016 2016