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: rs1057517662
rs1057517662
SPARC
1 1.000 5 151667555 missense variant C/T snv 4.0E-06 7.0E-06 0.800 0
dbSNP: rs1057517663
rs1057517663
SPARC
1 1.000 5 151664183 missense variant C/T snv 0.800 0