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Variant (rsID / SNP)

rs770674650

RET

rs770674650 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RET. Location: chromosome 10, position 43,615,133. 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
10:43615133
Cytoband
10q11.21
HGVS
NM_020975.6(RET):c.2547C>T (p.Gly849_Asp850=)
Allele change
Synonymous_G849G

Associated conditions / phenotypes

Multiple endocrine neoplasia, type 2|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.