VPS13B Chromosome 8

Vacuolar protein sorting 13 homolog B
976 variants 976 Health Risk

Upload your DNA to see your personal genotypes for variants in VPS13B.

What This Gene Does
This gene encodes a potential transmembrane protein that may function in vesicle-mediated transport and sorting of proteins within the cell. This protein may play a role in the development and the function of the eye, hematological system, and central nervous system. Mutations in this gene have been associated with Cohen syndrome. Multiple splice variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Bridge-like lipid transfer protein family
Locus Type
gene with protein product
Location
8q22.2
Ensembl
ENSG00000132549
Associated Conditions (34)
Cohen syndrome
Inborn genetic diseases
VPS13B-related disorder
Abnormal brain morphology
Intellectual disability
Ovarian serous cystadenocarcinoma
Thyroid cancer
nonmedullary
1
Lung cancer
Gastric cancer
Adrenocortical carcinoma
hereditary
Early onset severe obesity
Familial cancer of breast
Malignant tumor of urinary bladder
Chronic lymphocytic leukemia/small lymphocytic lymphoma
High myopia
early-onset
Ovarian cancer
+14 more conditions
Key Variants
RS1019355776
Conflicting classifications of pathogenicity
Cohen syndrome, Inborn genetic diseases, Cohen syndrome
Health Risk
RS1046756662
Conflicting classifications of pathogenicity
Cohen syndrome, VPS13B-related disorder, Cohen syndrome
Health Risk
RS1057519183
Conflicting classifications of pathogenicity
Cohen syndrome, Cohen syndrome
Health Risk
RS1060499779
Conflicting classifications of pathogenicity
Abnormal brain morphology, Cohen syndrome, Abnormal brain morphology
Health Risk
RS112634620
Conflicting classifications of pathogenicity
Cohen syndrome, Inborn genetic diseases, VPS13B-related disorder
Health Risk
RS116546060
Conflicting classifications of pathogenicity
Cohen syndrome, Inborn genetic diseases, Cohen syndrome
Health Risk
RS117148013
Conflicting classifications of pathogenicity
Cohen syndrome, Inborn genetic diseases, VPS13B-related disorder
Health Risk
RS1178600682
Conflicting classifications of pathogenicity
Cohen syndrome, Inborn genetic diseases, Cohen syndrome
Health Risk
RS117934093
Conflicting classifications of pathogenicity
Cohen syndrome, VPS13B-related disorder, Cohen syndrome
Health Risk
RS1180933570
Conflicting classifications of pathogenicity
Cohen syndrome, Inborn genetic diseases, Cohen syndrome
Health Risk
RS118158347
Conflicting classifications of pathogenicity
Cohen syndrome, Inborn genetic diseases, VPS13B-related disorder
Health Risk
RS1225418115
Conflicting classifications of pathogenicity
Cohen syndrome, Inborn genetic diseases, Cohen syndrome
Health Risk
All Variants (976)
RSID Category Clinical Significance Conditions
RS386834056 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS386834059 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS386834063 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS386834065 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS386834073 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS386834075 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS386834076 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS386834079 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS386834081 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS386834082 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome, Cohen syndrome
RS386834085 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS386834087 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS386834089 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS386834094 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS386834097 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS386834100 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS386834101 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS386834102 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS386834103 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS386834108 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS386834109 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS386834111 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS386834114 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS386834120 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome, Cohen syndrome
RS386834121 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS386834122 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS542757501 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS745404712 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome, Cohen syndrome
RS746521429 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS747363890 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome, Cohen syndrome
RS747644844 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS750003804 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome, Cohen syndrome
RS750092574 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS750609612 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS756013171 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome, Cohen syndrome
RS759374475 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome, Cohen syndrome
RS760207157 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS763079458 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome, Cohen syndrome
RS764225649 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome, Cohen syndrome
RS766409208 Health Risk Likely pathogenic Cohen syndrome, Lung cancer, Cohen syndrome
RS768342041 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome, Cohen syndrome
RS768406797 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS768801125 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS775729058 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS780902262 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome, Cohen syndrome
RS910393433 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS930144563 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS988245745 Health Risk Likely pathogenic Cohen syndrome, Cohen syndrome
RS1014496937 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1057516245 Health Risk Pathogenic Cohen syndrome, Cohen syndrome
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