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: rs397515798
rs397515798
1.000 0.160 15 48474599 missense variant C/G;T snv
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
0.700 1.000 2 1999 2001
dbSNP: rs397515817
rs397515817
1.000 0.160 15 48464009 missense variant C/T snv
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
0.700 1.000 2 2001 2001
dbSNP: rs397515823
rs397515823
1.000 0.160 15 48452595 missense variant C/A;T snv
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
0.700 1.000 2 2006 2011
dbSNP: rs397515859
rs397515859
1.000 0.160 15 48415632 missense variant C/T snv
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
0.700 1.000 2 2002 2007
dbSNP: rs587782944
rs587782944
1.000 0.160 15 48513641 missense variant C/T snv
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
0.700 1.000 2 2011 2011
dbSNP: rs727503056
rs727503056
1.000 0.160 15 48467967 frameshift variant GTACCCCAGGCTTTACCCAGAGAACAGCAGCAGGAAGCTTTGGA/- delins
CUI: C0265313
Disease: Weill-Marchesani syndrome
Weill-Marchesani syndrome
0.700 1.000 2 2002 2003
dbSNP: rs869025404
rs869025404
1.000 0.160 15 48505076 missense variant A/G snv
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
0.700 1.000 2 1999 2012
dbSNP: rs869025415
rs869025415
1.000 0.160 15 48425401 missense variant T/C snv
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
0.700 1.000 2 2002 2007
dbSNP: rs869025419
rs869025419
1.000 0.160 15 48432865 splice donor variant C/G;T snv
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
0.700 1.000 2 2007 2015
dbSNP: rs112911555
rs112911555
1.000 0.160 15 48490072 missense variant C/T snv 4.0E-06
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
0.700 1.000 1 2009 2009
dbSNP: rs113086760
rs113086760
1.000 0.160 15 48448851 missense variant C/T snv
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
0.700 1.000 1 2015 2015
dbSNP: rs1555395756
rs1555395756
1.000 0.160 15 48445432 frameshift variant A/- delins
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
0.700 1.000 1 2016 2016
dbSNP: rs1555397655
rs1555397655
1.000 0.160 15 48474294 frameshift variant ACAG/- delins
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
0.700 1.000 1 2013 2013
dbSNP: rs1555398394
rs1555398394
1.000 0.160 15 48485430 missense variant T/C snv
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
0.700 1.000 1 2005 2005
dbSNP: rs1555399165
rs1555399165
1.000 0.160 15 48495243 missense variant A/G;T snv
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
0.700 1.000 1 2019 2019
dbSNP: rs1555404803
rs1555404803
1.000 0.160 15 48596318 missense variant C/A snv
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
0.700 1.000 1 2020 2020
dbSNP: rs1566891645
rs1566891645
1.000 0.160 15 48421563 missense variant C/T snv
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
0.700 1.000 1 2019 2019
dbSNP: rs1566891701
rs1566891701
1.000 15 48421675 missense variant A/G snv
Familial thoracic aortic aneurysm and aortic dissection
0.700 1.000 1 2019 2019
dbSNP: rs1566895225
rs1566895225
1.000 0.160 15 48434596 frameshift variant -/C delins
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
0.700 1.000 1 2019 2019
dbSNP: rs1566898399
rs1566898399
1.000 0.160 15 48445388 frameshift variant T/- del
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
0.700 1.000 1 2019 2019
dbSNP: rs1566903931
rs1566903931
1.000 0.120 15 48465619 missense variant AC/CA mnv
CUI: C1858556
Disease: OVERLAP CONNECTIVE TISSUE DISEASE
OVERLAP CONNECTIVE TISSUE DISEASE
0.700 1.000 1 2005 2005
dbSNP: rs1566904011
rs1566904011
1.000 0.160 15 48465825 frameshift variant C/- delins
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
0.700 1.000 1 2019 2019
dbSNP: rs1566906537
rs1566906537
1.000 0.160 15 48474579 missense variant A/C snv
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
0.700 1.000 1 2019 2019
dbSNP: rs1566908956
rs1566908956
1.000 0.160 15 48485487 missense variant T/A snv
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
0.700 1.000 1 2019 2019
dbSNP: rs1566909766
rs1566909766
1.000 0.160 15 48488118 missense variant C/T snv
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome
0.700 1.000 1 2019 2019