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: rs587777695
rs587777695
0.925 0.120 5 61544156 missense variant C/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 3 2014 2017
dbSNP: rs869320713
rs869320713
0.851 0.120 10 248370 missense variant G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 1 2014 2014
dbSNP: rs797044854
rs797044854
0.925 10 252459 missense variant C/A;T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 8 2006 2015
dbSNP: rs1553961516
rs1553961516
1.000 2 144398578 stop gained G/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 8 2005 2017
dbSNP: rs587784570
rs587784570
0.925 0.280 2 144401292 stop gained G/A;C snv 4.0E-06
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 8 2005 2017
dbSNP: rs1555933851
rs1555933851
1.000 X 64919152 frameshift variant -/G delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 2 2013 2015
dbSNP: rs797044863
rs797044863
1.000 X 64921894 stop gained G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 2 2013 2015
dbSNP: rs1553794464
rs1553794464
1.000 3 114350821 frameshift variant -/C delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 7 2009 2017
dbSNP: rs1553270522
rs1553270522
1.000 1 244054804 frameshift variant GATGA/- delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 26 1997 2017
dbSNP: rs797044885
rs797044885
0.925 1 244055156 missense variant A/G snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 26 1997 2017
dbSNP: rs797044806
rs797044806
0.925 17 50354465 frameshift variant -/C delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 4 2015 2018
dbSNP: rs769391314
rs769391314
1.000 16 17109015 stop gained C/A;T snv 5.5E-06; 1.1E-05
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 5 2014 2017
dbSNP: rs121908119
rs121908119
0.763 0.200 2 218882368 stop gained C/A snv 6.2E-04 8.5E-04
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 6 2007 2017
dbSNP: rs1557084120
rs1557084120
1.000 X 49075874 stop gained G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 10 2010 2017
dbSNP: rs387907329
rs387907329
0.827 0.200 X 49075573 stop gained G/A;T snv 5.5E-06
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 10 2010 2017
dbSNP: rs886041382
rs886041382
0.925 0.080 X 49078077 stop gained G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 10 2010 2017
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: rs864321692
rs864321692
WAC
0.925 10 28583498 stop gained C/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 6 2011 2016
dbSNP: rs120074152
rs120074152
0.925 0.320 8 99384294 stop gained C/T snv 4.0E-06 7.0E-06
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 12 1998 2015
dbSNP: rs1554884733
rs1554884733
1.000 8 99641974 frameshift variant -/GTCC delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 12 1998 2015
dbSNP: rs886041185
rs886041185
0.925 0.320 8 99835295 frameshift variant -/A delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 12 1998 2015
dbSNP: rs587777585
rs587777585
0.882 6 30918851 missense variant C/G;T snv 2.4E-05
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 6 2011 2017
dbSNP: rs1555922391
rs1555922391
1.000 X 41151058 splice donor variant G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 5 2014 2017
dbSNP: rs1555933969
rs1555933969
1.000 X 41216161 frameshift variant T/- delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 0
dbSNP: rs1304422857
rs1304422857
1.000 12 109511304 splice donor variant G/A;T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 8 2003 2018