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: rs121909583
rs121909583
C3
2 0.925 0.120 19 6709754 missense variant C/T snv 0.800 1.000 4 2008 2010
dbSNP: rs121909584
rs121909584
C3
1 1.000 19 6693033 missense variant G/A snv 0.800 1.000 4 2008 2010
dbSNP: rs121909585
rs121909585
C3
4 0.925 0.120 19 6692971 missense variant C/T snv 0.800 1.000 4 2008 2010
dbSNP: rs771353792
rs771353792
C3
1 1.000 19 6709755 missense variant G/A snv 4.0E-06 0.700 1.000 2 2008 2010
dbSNP: rs794729228
rs794729228
C3
1 1.000 19 6714208 missense variant G/A snv 0.700 1.000 1 2008 2008
dbSNP: rs117793540
rs117793540
C3
2 0.925 0.040 19 6707118 missense variant G/A snv 2.2E-03 1.9E-03 0.700 0
dbSNP: rs121909586
rs121909586
C3
1 1.000 19 6697673 stop gained G/A;C snv 0.700 0
dbSNP: rs775015499
rs775015499
C3
1 1.000 19 6685049 missense variant C/A;T snv 4.0E-06; 1.6E-05 0.700 0