Source: ALL
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: rs1364382189
rs1364382189
GPI
2 0.925 0.080 19 34399571 missense variant C/T snv 0.010 1.000 1 2018 2018
dbSNP: rs374583873
rs374583873
GPI
2 0.925 0.080 19 34399616 missense variant C/T snv 4.0E-06 0.010 1.000 1 2012 2012