RS143313688 CTSF

Health Risk Chr 11:66566336
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What This Variant Does
"Exome Sequencing of Familial Bipolar Disorder. The minor allele of this SNP is one of 84 rare varian..."
Associated Conditions
Neuronal ceroid lipofuscinosis 13
Inborn genetic diseases
CTSF-related disorder
Neuronal ceroid lipofuscinosis 13
Inborn genetic diseases
CTSF-related disorder
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
CTSF protein levels A OR: 1.27 1E-178 PubMed
Other Variants in CTSF
rs397514731 rs397514732 rs397514733 rs753084727 rs797045136 rs141915593 rs148611356 rs1555058286 rs141345438 rs573483617
Ask Dr. Hemsworth about this variant