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: 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: rs1553693712
rs1553693712
1.000 3 9734167 frameshift variant TT/- delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 2 2017 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: rs587777644
rs587777644
0.925 17 76733060 frameshift variant CACT/- delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 2 2014 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: rs762904815
rs762904815
1.000 3 9744394 frameshift variant C/-;CC;CCC delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 2 2017 2017
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: 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: rs1057519413
rs1057519413
0.925 0.120 15 40729955 missense variant G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 3 2014 2015
dbSNP: rs1131690805
rs1131690805
0.925 6 26156815 frameshift variant -/G delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 3 2013 2017
dbSNP: rs1366421988
rs1366421988
1.000 8 1771146 missense variant G/A;T snv 4.0E-06
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 3 2015 2017
dbSNP: rs148234606
rs148234606
0.925 8 144360604 missense variant T/C snv 7.0E-05 7.7E-05
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 3 2012 2016
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: rs1553766262
rs1553766262
1.000 3 122257279 missense variant C/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 3 2010 2017
dbSNP: rs1554260888
rs1554260888
1.000 6 133456594 frameshift variant A/- del
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 3 2005 2016
dbSNP: rs1554672061
rs1554672061
1.000 9 35793897 splice acceptor variant G/C snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 3 2004 2015
dbSNP: rs1555537637
rs1555537637
1.000 17 4533107 frameshift variant CC/T delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 3 2009 2017
dbSNP: rs1555750721
rs1555750721
ERF
1.000 19 42249327 frameshift variant G/- delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 3 2010 2017
dbSNP: rs1556026984
rs1556026984
0.925 0.120 X 134475194 missense variant G/C snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 3 2014 2015
dbSNP: rs201091657
rs201091657
1.000 3 122261684 missense variant G/A;T snv 1.6E-05
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 3 2010 2017
dbSNP: rs201108965
rs201108965
0.851 0.320 11 61393965 missense variant G/A;T snv 8.0E-06; 1.7E-04
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 3 2010 2015
dbSNP: rs386834124
rs386834124
0.925 0.120 8 1771263 missense variant G/A snv 2.8E-05 1.4E-05
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 3 2015 2017
dbSNP: rs567573386
rs567573386
0.882 0.120 16 56484820 stop gained G/A snv 3.2E-05 1.4E-05
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 3 2007 2013
dbSNP: rs587777357
rs587777357
0.925 6 30724263 missense variant G/A snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 3 2012 2015
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