RINT1 Chromosome 7

RAD50 interactor 1
93 variants 93 Health Risk

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What This Gene Does
This gene encodes a protein first identified for its ability to interact with the RAD50 double strand break repair protein, with the resulting interaction implicated in the regulation of cell cycle progression and telomere length. The encoded protein may also play a role in trafficking of cellular cargo from the endosome to the trans-Golgi network. Mutations in this gene may be associated with breast cancer in human patients. [provided by RefSeq, Oct 2016]
Gene Info
Gene Group
NRZ tethering complex
Locus Type
gene with protein product
Location
7q22.3
Ensembl
ENSG00000135249
Associated Conditions (8)
Infantile liver failure syndrome 3
Thyroid cancer
nonmedullary
1
Hereditary breast ovarian cancer syndrome
RINT1-related disorder
Fulminant hepatic failure
Familial ovarian cancer
Key Variants
All Variants (93)
RSID Category Clinical Significance Conditions
RS1017536954 Health Risk Conflicting classifications of pathogenicity
RS1301146115 Health Risk Conflicting classifications of pathogenicity Infantile liver failure syndrome 3, Infantile liver failure syndrome 3
RS1350432366 Health Risk Conflicting classifications of pathogenicity
RS1352349454 Health Risk Conflicting classifications of pathogenicity
RS138345617 Health Risk Conflicting classifications of pathogenicity Infantile liver failure syndrome 3, Infantile liver failure syndrome 3
RS139214585 Health Risk Conflicting classifications of pathogenicity
RS1414090114 Health Risk Conflicting classifications of pathogenicity
RS144994876 Health Risk Conflicting classifications of pathogenicity
RS144996870 Health Risk Conflicting classifications of pathogenicity
RS145688388 Health Risk Conflicting classifications of pathogenicity
RS151055286 Health Risk Conflicting classifications of pathogenicity Thyroid cancer, nonmedullary, 1
RS1562853874 Health Risk Conflicting classifications of pathogenicity
RS1586216562 Health Risk Conflicting classifications of pathogenicity
RS1586272463 Health Risk Conflicting classifications of pathogenicity
RS1790695219 Health Risk Conflicting classifications of pathogenicity
RS1790697157 Health Risk Conflicting classifications of pathogenicity
RS1790698966 Health Risk Conflicting classifications of pathogenicity
RS1791557727 Health Risk Conflicting classifications of pathogenicity
RS1791671293 Health Risk Conflicting classifications of pathogenicity Hereditary breast ovarian cancer syndrome, Hereditary breast ovarian cancer syndrome
RS199512216 Health Risk Conflicting classifications of pathogenicity
RS199535472 Health Risk Conflicting classifications of pathogenicity
RS200970042 Health Risk Conflicting classifications of pathogenicity
RS201892348 Health Risk Conflicting classifications of pathogenicity
RS201898612 Health Risk Conflicting classifications of pathogenicity
RS202189669 Health Risk Conflicting classifications of pathogenicity Infantile liver failure syndrome 3, Infantile liver failure syndrome 3
RS2485150163 Health Risk Conflicting classifications of pathogenicity
RS2485181856 Health Risk Conflicting classifications of pathogenicity
RS374836052 Health Risk Conflicting classifications of pathogenicity Infantile liver failure syndrome 3, Infantile liver failure syndrome 3
RS566923305 Health Risk Conflicting classifications of pathogenicity
RS749732262 Health Risk Conflicting classifications of pathogenicity
RS750920467 Health Risk Conflicting classifications of pathogenicity
RS755970186 Health Risk Conflicting classifications of pathogenicity
RS756001839 Health Risk Conflicting classifications of pathogenicity
RS756236683 Health Risk Conflicting classifications of pathogenicity
RS757668486 Health Risk Conflicting classifications of pathogenicity
RS758536777 Health Risk Conflicting classifications of pathogenicity
RS759853907 Health Risk Conflicting classifications of pathogenicity RINT1-related disorder, Infantile liver failure syndrome 3, RINT1-related disorder
RS759899058 Health Risk Conflicting classifications of pathogenicity
RS763099446 Health Risk Conflicting classifications of pathogenicity
RS764298491 Health Risk Conflicting classifications of pathogenicity Hereditary breast ovarian cancer syndrome, Hereditary breast ovarian cancer syndrome
RS765034316 Health Risk Conflicting classifications of pathogenicity
RS766540386 Health Risk Conflicting classifications of pathogenicity
RS767516791 Health Risk Conflicting classifications of pathogenicity
RS767609311 Health Risk Conflicting classifications of pathogenicity
RS767925162 Health Risk Conflicting classifications of pathogenicity
RS768627748 Health Risk Conflicting classifications of pathogenicity
RS770595233 Health Risk Conflicting classifications of pathogenicity
RS771302691 Health Risk Conflicting classifications of pathogenicity
RS774464035 Health Risk Conflicting classifications of pathogenicity
RS777242801 Health Risk Conflicting classifications of pathogenicity
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