Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121908674
rs121908674
0.882 0.160 11 68410076 missense variant C/G;T snv
EXUDATIVE VITREORETINOPATHY 4 (disorder)
0.700 1.000 8 2004 2014
dbSNP: rs1245625202
rs1245625202
1.000 0.080 11 68390000 missense variant A/C;G snv 8.0E-06; 4.0E-06
EXUDATIVE VITREORETINOPATHY 4 (disorder)
0.700 1.000 8 2004 2014
dbSNP: rs1398692057
rs1398692057
1.000 0.080 11 68413740 missense variant C/T snv 7.0E-06
EXUDATIVE VITREORETINOPATHY 4 (disorder)
0.700 1.000 8 2004 2014
dbSNP: rs28939709
rs28939709
0.925 0.080 11 68436987 missense variant G/A snv 8.0E-06
EXUDATIVE VITREORETINOPATHY 4 (disorder)
0.700 1.000 8 2004 2014
dbSNP: rs765952535
rs765952535
1.000 0.080 11 68411530 missense variant C/T snv 1.6E-05 1.4E-05
EXUDATIVE VITREORETINOPATHY 4 (disorder)
0.700 1.000 8 2004 2014
dbSNP: rs768615287
rs768615287
0.925 0.160 11 68429695 missense variant G/A;T snv 4.0E-06
EXUDATIVE VITREORETINOPATHY 4 (disorder)
0.700 1.000 8 2004 2014
dbSNP: rs80358305
rs80358305
0.882 0.160 11 68348188 missense variant C/T snv
EXUDATIVE VITREORETINOPATHY 4 (disorder)
0.700 1.000 8 2004 2014
dbSNP: rs80358306
rs80358306
1.000 0.080 11 68357679 missense variant C/T snv 3.9E-04 5.0E-04
EXUDATIVE VITREORETINOPATHY 4 (disorder)
0.700 1.000 8 2004 2014
dbSNP: rs80358308
rs80358308
0.925 0.080 11 68386630 missense variant C/T snv 2.0E-05 7.0E-06
EXUDATIVE VITREORETINOPATHY 4 (disorder)
0.700 1.000 8 2004 2014
dbSNP: rs80358309
rs80358309
1.000 0.080 11 68390032 missense variant G/A snv 4.0E-06
EXUDATIVE VITREORETINOPATHY 4 (disorder)
0.700 1.000 8 2004 2014
dbSNP: rs80358310
rs80358310
1.000 0.080 11 68403502 missense variant C/T snv 1.2E-05
EXUDATIVE VITREORETINOPATHY 4 (disorder)
0.700 1.000 8 2004 2014
dbSNP: rs80358311
rs80358311
1.000 0.080 11 68403546 missense variant G/A snv 4.0E-06 7.0E-06
EXUDATIVE VITREORETINOPATHY 4 (disorder)
0.700 1.000 8 2004 2014
dbSNP: rs80358312
rs80358312
0.925 0.080 11 68403607 missense variant G/A snv 7.0E-06
EXUDATIVE VITREORETINOPATHY 4 (disorder)
0.700 1.000 8 2004 2014
dbSNP: rs80358313
rs80358313
0.882 0.160 11 68406550 missense variant G/A;C;T snv 1.2E-05; 1.2E-05; 3.2E-05
EXUDATIVE VITREORETINOPATHY 4 (disorder)
0.700 1.000 8 2004 2014
dbSNP: rs80358314
rs80358314
1.000 0.080 11 68406572 missense variant T/G snv
EXUDATIVE VITREORETINOPATHY 4 (disorder)
0.700 1.000 8 2004 2014
dbSNP: rs80358316
rs80358316
1.000 0.080 11 68411509 missense variant A/G snv 8.0E-06 2.1E-05
EXUDATIVE VITREORETINOPATHY 4 (disorder)
0.700 1.000 8 2004 2014
dbSNP: rs80358317
rs80358317
1.000 0.080 11 68425226 missense variant A/G snv 6.4E-04 2.4E-04
EXUDATIVE VITREORETINOPATHY 4 (disorder)
0.700 1.000 8 2004 2014
dbSNP: rs80358318
rs80358318
1.000 0.080 11 68426052 missense variant T/C snv
EXUDATIVE VITREORETINOPATHY 4 (disorder)
0.700 1.000 8 2004 2014
dbSNP: rs121908664
rs121908664
1.000 0.120 11 68389949 missense variant G/A snv
CUI: C0432252
Disease: Osteoporosis with pseudoglioma
Osteoporosis with pseudoglioma
0.800 1.000 5 2001 2008
dbSNP: rs121908665
rs121908665
1.000 0.120 11 68403606 missense variant C/T snv
CUI: C0432252
Disease: Osteoporosis with pseudoglioma
Osteoporosis with pseudoglioma
0.800 1.000 5 2001 2008
dbSNP: rs121908668
rs121908668
0.882 0.240 11 68357673 missense variant G/T snv
BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 1
0.700 1.000 5 2002 2007
dbSNP: rs1219101402
rs1219101402
1.000 0.120 11 68365607 missense variant C/T snv 7.0E-06
CUI: C0432252
Disease: Osteoporosis with pseudoglioma
Osteoporosis with pseudoglioma
0.700 1.000 5 2001 2008
dbSNP: rs201320326
rs201320326
1.000 0.120 11 68386499 missense variant C/A;T snv 2.2E-04
CUI: C0432252
Disease: Osteoporosis with pseudoglioma
Osteoporosis with pseudoglioma
0.700 1.000 5 2001 2008
dbSNP: rs377258285
rs377258285
1.000 0.120 11 68425202 missense variant C/T snv 5.6E-05 6.3E-05
CUI: C0432252
Disease: Osteoporosis with pseudoglioma
Osteoporosis with pseudoglioma
0.700 1.000 5 2001 2008
dbSNP: rs397514665
rs397514665
1.000 0.120 11 68363791 missense variant C/T snv 1.2E-05
CUI: C0432252
Disease: Osteoporosis with pseudoglioma
Osteoporosis with pseudoglioma
0.800 1.000 5 2001 2008