SMAD6 Chromosome 15

SMAD family member 6
111 variants 111 Health Risk

Upload your DNA to see your personal genotypes for variants in SMAD6.

What This Gene Does
The protein encoded by this gene belongs to the SMAD family of proteins, which are related to Drosophila 'mothers against decapentaplegic' (Mad) and C. elegans Sma. SMAD proteins are signal transducers and transcriptional modulators that mediate multiple signaling pathways. This protein functions in the negative regulation of BMP and TGF-beta/activin-signalling. Multiple transcript variants have been found for this gene.[provided by RefSeq, Sep 2014]
Gene Info
Gene Group
SMAD family
Locus Type
gene with protein product
Location
15q22.31
Ensembl
ENSG00000137834
Associated Conditions (20)
Radioulnar synostosis
Craniosynostosis 7
Aortic valve disease 2
CRANIOSYNOSTOSIS 7
SUSCEPTIBILITY TO
Frontal bossing
Premature closure of fontanelles
Plagiocephaly
Thoracic aortic aneurysm
SMAD6-related disorder
Aneurysm-osteoarthritis syndrome
Aortic valve disease 1
Polydactyly
nonsyndromic
susceptibility to
Inborn genetic diseases
Craniosynostosis syndrome
Abnormal axial skeleton morphology
Heart
malformation of
Key Variants
RS1006397889
Conflicting classifications of pathogenicity
Radioulnar synostosis, Craniosynostosis 7, Aortic valve disease 2
Health Risk
RS1011464295
Conflicting classifications of pathogenicity
Aortic valve disease 2, Aortic valve disease 2
Health Risk
RS1056072996
Conflicting classifications of pathogenicity
Aortic valve disease 2, Aortic valve disease 2
Health Risk
RS1064793003
Conflicting classifications of pathogenicity
CRANIOSYNOSTOSIS 7, SUSCEPTIBILITY TO, Aortic valve disease 2
Health Risk
RS1160042861
Conflicting classifications of pathogenicity
Radioulnar synostosis, Aortic valve disease 2, Radioulnar synostosis
Health Risk
RS1199495614
Conflicting classifications of pathogenicity
Radioulnar synostosis, Aortic valve disease 2, Radioulnar synostosis
Health Risk
RS1213841516
Conflicting classifications of pathogenicity
Radioulnar synostosis, Frontal bossing, Premature closure of fontanelles
Health Risk
RS1235097131
Conflicting classifications of pathogenicity
Aortic valve disease 2, Radioulnar synostosis, SMAD6-related disorder
Health Risk
RS1241989233
Conflicting classifications of pathogenicity
Aortic valve disease 2, Aortic valve disease 2
Health Risk
RS1246889300
Conflicting classifications of pathogenicity
Aneurysm-osteoarthritis syndrome, Aortic valve disease 2, Aortic valve disease 1
Health Risk
RS1353173742
Conflicting classifications of pathogenicity
Health Risk
RS1409145798
Conflicting classifications of pathogenicity
Polydactyly, Radioulnar synostosis, Aortic valve disease 2
Health Risk
All Variants (111)
RSID Category Clinical Significance Conditions
RS1006397889 Health Risk Conflicting classifications of pathogenicity Radioulnar synostosis, Craniosynostosis 7, Aortic valve disease 2
RS1011464295 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Aortic valve disease 2
RS1056072996 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Aortic valve disease 2
RS1064793003 Health Risk Conflicting classifications of pathogenicity CRANIOSYNOSTOSIS 7, SUSCEPTIBILITY TO, Aortic valve disease 2
RS1160042861 Health Risk Conflicting classifications of pathogenicity Radioulnar synostosis, Aortic valve disease 2, Radioulnar synostosis
RS1199495614 Health Risk Conflicting classifications of pathogenicity Radioulnar synostosis, Aortic valve disease 2, Radioulnar synostosis
RS1213841516 Health Risk Conflicting classifications of pathogenicity Radioulnar synostosis, Frontal bossing, Premature closure of fontanelles
RS1235097131 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Radioulnar synostosis, SMAD6-related disorder
RS1241989233 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Aortic valve disease 2
RS1246889300 Health Risk Conflicting classifications of pathogenicity Aneurysm-osteoarthritis syndrome, Aortic valve disease 2, Aortic valve disease 1
RS1353173742 Health Risk Conflicting classifications of pathogenicity
RS1409145798 Health Risk Conflicting classifications of pathogenicity Polydactyly, Radioulnar synostosis, Aortic valve disease 2
RS1419095990 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 1, Aortic valve disease 2, Aortic valve disease 1
RS144403747 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Aortic valve disease 2
RS1447391811 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Aortic valve disease 2
RS149949971 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Aortic valve disease 2
RS1567092071 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 1, Aortic valve disease 2, Aortic valve disease 1
RS1595756640 Health Risk Conflicting classifications of pathogenicity Radioulnar synostosis, Aortic valve disease 2, Radioulnar synostosis
RS1893047812 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Aortic valve disease 2
RS1894556452 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Radioulnar synostosis, nonsyndromic
RS199531653 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Aortic valve disease 2
RS199822239 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Craniosynostosis 7, SMAD6-related disorder
RS200004068 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Inborn genetic diseases, Aortic valve disease 2
RS200374822 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Craniosynostosis 7, Inborn genetic diseases
RS201098141 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Inborn genetic diseases, Aortic valve disease 2
RS2140581496 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Aortic valve disease 2
RS2140596524 Health Risk Conflicting classifications of pathogenicity Radioulnar synostosis, nonsyndromic, susceptibility to
RS2541897696 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Aortic valve disease 2
RS2545310288 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, SMAD6-related disorder, Aortic valve disease 2
RS373376338 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Inborn genetic diseases, SMAD6-related disorder
RS373836386 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Aortic valve disease 2
RS529866697 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Inborn genetic diseases, Aortic valve disease 2
RS532621952 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Inborn genetic diseases, Aortic valve disease 2
RS748622672 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Inborn genetic diseases, Aortic valve disease 2
RS749741980 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Inborn genetic diseases, Aortic valve disease 2
RS751440011 Health Risk Conflicting classifications of pathogenicity Craniosynostosis 7, Aortic valve disease 2, Craniosynostosis 7
RS756752655 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Inborn genetic diseases, Aortic valve disease 2
RS759468399 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Inborn genetic diseases, Aortic valve disease 2
RS760571406 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Aortic valve disease 2
RS766270982 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Aortic valve disease 2
RS769605183 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Craniosynostosis 7, Aortic valve disease 2
RS776347265 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Inborn genetic diseases, Aortic valve disease 2
RS779805606 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Aortic valve disease 2
RS80232004 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Aortic valve disease 2
RS952876781 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, SMAD6-related disorder, Aortic valve disease 2
RS958818801 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Radioulnar synostosis, Craniosynostosis syndrome
RS965061234 Health Risk Conflicting classifications of pathogenicity Aortic valve disease 2, Radioulnar synostosis, Aortic valve disease 2
RS1057517824 Health Risk Likely pathogenic
RS1255802415 Health Risk Likely pathogenic Radioulnar synostosis, Radioulnar synostosis
RS1325349483 Health Risk Likely pathogenic Aortic valve disease 2, Aortic valve disease 2
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