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: rs1555985372
rs1555985372
1.000 X 100407591 frameshift variant -/C delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 16 2008 2017
dbSNP: rs1553259529
rs1553259529
MPZ
1.000 1 161306152 frameshift variant -/C delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 14 1998 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: rs1557099144
rs1557099144
1.000 X 53985131 frameshift variant -/C delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 7 2005 2014
dbSNP: rs796065308
rs796065308
0.925 0.160 11 822522 frameshift variant -/C delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 6 2008 2016
dbSNP: rs797044677
rs797044677
1.000 2 232540049 frameshift variant -/C delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 5 2006 2016
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: rs1554120939
rs1554120939
1.000 6 33435269 frameshift variant -/CACA delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 18 2004 2017
dbSNP: rs1555046428
rs1555046428
1.000 11 118503078 frameshift variant -/CAGAT delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 22 1989 2017
dbSNP: rs1555184787
rs1555184787
1.000 12 49022591 frameshift variant -/G delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 25 1988 2017
dbSNP: rs1554236054
rs1554236054
1.000 6 157201481 frameshift variant -/G delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 20 1984 2017
dbSNP: rs1555321405
rs1555321405
1.000 14 28768359 frameshift variant -/G delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 15 1989 2017
dbSNP: rs1555447011
rs1555447011
1.000 16 2093886 frameshift variant -/G delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 13 1999 2015
dbSNP: rs775499191
rs775499191
1.000 1 183286706 frameshift variant -/G delins 4.0E-06; 4.0E-06
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 13 2002 2016
dbSNP: rs767858333
rs767858333
1.000 10 127042665 frameshift variant -/G delins 4.0E-06; 1.6E-05
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 10 1988 2017
dbSNP: rs1555912897
rs1555912897
1.000 20 32436833 frameshift variant -/G delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 7 2004 2015
dbSNP: rs34927195
rs34927195
1.000 X 71147958 frameshift variant -/G delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 4 2003 2014
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: 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: rs797044884
rs797044884
0.925 17 59677123 frameshift variant -/GA delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 23 1976 2017
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: rs1555186842
rs1555186842
1.000 12 49030285 frameshift variant -/GTGCCCTT delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 25 1988 2017
dbSNP: rs1555393647
rs1555393647
1.000 15 48412588 frameshift variant -/T delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 29 1986 2016
dbSNP: rs1555990816
rs1555990816
1.000 21 37505344 frameshift variant -/T delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 18 1990 2016
dbSNP: rs1555528558
rs1555528558
1.000 16 89283207 frameshift variant -/T delins
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 17 2004 2017