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: rs1054627
rs1054627
3 1.000 0.080 4 87811540 missense variant G/A snv 0.30 0.24 0.010 1.000 1 2015 2015
dbSNP: rs17013181
rs17013181
1 1.000 0.080 4 87811611 missense variant A/G snv 0.21 0.26 0.010 1.000 1 2015 2015