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: rs387906999
rs387906999
GIPC3
1 1.000 0.120 19 3589910 missense variant T/G snv 0.800 1.000 2 2011 2011
dbSNP: rs387907001
rs387907001
GIPC3
1 1.000 0.120 19 3589892 missense variant G/A snv 0.800 1.000 2 2011 2011
dbSNP: rs387907002
rs387907002
GIPC3
1 1.000 0.120 19 3586967 missense variant C/A;T snv 0.800 1.000 2 2011 2011
dbSNP: rs1214652710
rs1214652710
GIPC3
1 1.000 0.120 19 3586533 missense variant G/C snv 4.0E-06 7.0E-06 0.700 1.000 2 2011 2011
dbSNP: rs761543680
rs761543680
GIPC3
1 1.000 0.120 19 3589512 missense variant C/T snv 4.0E-05 0.700 1.000 2 2011 2011
dbSNP: rs763523474
rs763523474
GIPC3
1 1.000 0.120 19 3586550 missense variant G/A;C snv 1.2E-05; 4.0E-06 0.700 1.000 2 2011 2011
dbSNP: rs1466835034
rs1466835034
GIPC3
1 1.000 0.120 19 3590188 stop lost T/C snv 4.8E-06 0.700 0
dbSNP: rs1568278651
rs1568278651
GIPC3
2 1.000 0.120 19 3589849 stop gained G/T snv 0.700 0
dbSNP: rs387907000
rs387907000
GIPC3
1 1.000 0.120 19 3590154 stop gained G/A snv 0.700 0
dbSNP: rs946085339
rs946085339
GIPC3
1 1.000 0.120 19 3585733 missense variant G/A;T snv 1.5E-05 0.700 0