Variant (rsID / SNP)

rs794728687

rs794728687 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RET. Location: chromosome 10, position 43,619,154. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

RETLikely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 10:43619154
Cytoband: 10q11.21
HGVS: NM_020975.6(RET):c.2837C>T (p.Thr946Ile)
Allele change: Missense_T946I

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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