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Variant (rsID / SNP)

rs765463636

RET

rs765463636 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RET. Location: chromosome 10, position 43,602,028. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

RETConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
10:43602028
Cytoband
10q11.21
HGVS
NM_020975.6(RET):c.1063+9G>A
Allele change
Silent

Associated conditions / phenotypes

Multiple endocrine neoplasia, type 2|Multiple endocrine neoplasia, type 2a|Multiple endocrine neoplasia, type 2b|Renal hypodysplasia/aplasia 1|Multiple endocrine neoplasia|Pheochromocytoma|Hirschsprung disease, susceptibility to, 1|Hereditary cancer-predisposing syndrome

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.