Source: CLINVAR

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: rs1553238271
rs1553238271
1.000 1 7661827 stop gained C/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 8 2006 2015
dbSNP: rs587776935
rs587776935
0.827 0.120 1 243505296 missense variant G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 8 1999 2017
dbSNP: rs121918243
rs121918243
0.882 0.160 1 45508848 missense variant G/A snv 1.7E-04 7.7E-05
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 7 2006 2015
dbSNP: rs1553262429
rs1553262429
1.000 1 228157838 stop gained G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 7 2004 2014
dbSNP: rs1553262430
rs1553262430
1.000 1 228157841 missense variant T/C snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 7 2004 2014
dbSNP: rs1283368278
rs1283368278
1.000 1 235401503 missense variant G/C snv 7.0E-06
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 6 1991 2016
dbSNP: rs1553234339
rs1553234339
1.000 1 103012412 splice donor variant C/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 6 1998 2014
dbSNP: rs372754256
rs372754256
1.000 1 152307855 stop gained G/C snv 4.7E-04 9.8E-05
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 6 1966 2013
dbSNP: rs387907186
rs387907186
0.925 0.120 1 149923670 frameshift variant G/-;GG delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 6 2007 2016
dbSNP: rs573518562
rs573518562
1.000 1 46192147 missense variant C/T snv 1.2E-05
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 6 2007 2016
dbSNP: rs746593718
rs746593718
1.000 1 235448437 stop gained -/AGTAA delins 2.0E-05 6.3E-05
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 6 1991 2016
dbSNP: rs387907306
rs387907306
SKI
0.925 0.160 1 2228866 missense variant G/A;T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 5 2005 2016
dbSNP: rs1193888919
rs1193888919
1.000 1 100107513 frameshift variant -/T delins 4.0E-06
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 4 2011 2014
dbSNP: rs1247427997
rs1247427997
1.000 1 165743244 stop gained G/A;T snv 4.0E-06; 4.0E-06
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 4 2010 2014
dbSNP: rs1553249737
rs1553249737
1.000 1 165743263 stop gained G/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 4 2010 2014
dbSNP: rs1026300967
rs1026300967
1.000 1 156868246 missense variant T/C snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 3 2012 2017
dbSNP: rs1553263326
rs1553263326
1.000 1 156881446 intron variant G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 3 2012 2017
dbSNP: rs1479675678
rs1479675678
1.000 1 62513588 stop gained G/A;C snv 7.0E-06
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 2 2006 2014
dbSNP: rs1553163123
rs1553163123
1.000 1 62528151 splice region variant C/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 2 2006 2014
dbSNP: rs757347274
rs757347274
0.925 1 235470849 splice donor variant C/T snv 4.8E-05 1.4E-05
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 2 2013 2014
dbSNP: rs1553353206
rs1553353206
1.000 1 224398525 frameshift variant CATTTAACAA/- delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 1 2017 2017
dbSNP: rs746480833
rs746480833
1.000 1 154569536 missense variant C/T snv 4.0E-06; 1.2E-05 2.8E-05
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 1 2017 2017
dbSNP: rs147001633
rs147001633
0.776 0.240 2 25234373 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 2.2E-04
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 36 1989 2018
dbSNP: rs1553583712
rs1553583712
1.000 2 165354339 frameshift variant GA/- del
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 34 1991 2017
dbSNP: rs796053162
rs796053162
0.882 0.080 2 165389123 missense variant G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 34 1991 2017