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: rs137853852
rs137853852
OCRL
1 1.000 0.200 X 129569368 missense variant A/G snv 0.700 1.000 10 1997 2011
dbSNP: rs137853853
rs137853853
OCRL
1 1.000 0.200 X 129569363 missense variant C/G;T snv 1.6E-05 0.700 1.000 10 1997 2011
dbSNP: rs137853854
rs137853854
OCRL
1 1.000 0.200 X 129562612 missense variant G/A snv 0.700 1.000 10 1997 2011
dbSNP: rs137853855
rs137853855
OCRL
1 1.000 0.200 X 129565789 missense variant G/A snv 0.700 1.000 10 1997 2011
dbSNP: rs137853856
rs137853856
OCRL
1 1.000 0.200 X 129565797 missense variant A/G snv 0.700 1.000 10 1997 2011
dbSNP: rs137853857
rs137853857
OCRL
1 1.000 0.200 X 129569290 missense variant G/A snv 0.700 1.000 10 1997 2011
dbSNP: rs137853858
rs137853858
OCRL
1 1.000 0.200 X 129569374 missense variant C/T snv 0.700 1.000 10 1997 2011
dbSNP: rs1556346316
rs1556346316
OCRL
1 1.000 0.200 X 129562444 stop gained C/T snv 0.700 1.000 3 1999 2017
dbSNP: rs1569458883
rs1569458883
OCRL
1 1.000 0.200 X 129558754 splice donor variant G/C snv 0.700 1.000 2 2011 2012
dbSNP: rs387906484
rs387906484
OCRL
1 1.000 0.200 X 129589905 stop gained C/T snv 0.700 1.000 1 1993 1993
dbSNP: rs935956958
rs935956958
OCRL
1 1.000 0.200 X 129588933 missense variant G/C;T snv 0.700 1.000 1 2007 2007
dbSNP: rs1057515577
rs1057515577
OCRL
1 1.000 0.200 X 129553302 intron variant A/G snv 0.700 0
dbSNP: rs1182741031
rs1182741031
OCRL
1 1.000 0.200 X 129575158 stop gained C/A;T snv 0.700 0
dbSNP: rs1556345889
rs1556345889
OCRL
1 1.000 0.200 X 129561212 frameshift variant -/T delins 0.700 0
dbSNP: rs1569463775
rs1569463775
OCRL
1 1.000 0.200 X 129588972 stop gained C/T snv 0.700 0
dbSNP: rs398123287
rs398123287
OCRL
1 1.000 0.200 X 129569295 stop gained C/G;T snv 5.4E-06 0.700 0
dbSNP: rs776743373
rs776743373
OCRL
2 0.925 0.200 X 129562373 intron variant G/A;T snv 2.2E-05 0.700 0