Source: BEFREE ×
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: rs759319721
rs759319721
PHKG1 ; SUMF2
1 1.000 0.120 7 56079533 missense variant G/C snv 8.0E-06 7.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs773695444
rs773695444
PHKG1 ; SUMF2
1 1.000 0.120 7 56079590 missense variant G/C snv 4.0E-06 0.010 1.000 1 2009 2009