Variant (rsID / SNP)

rs61742289

rs61742289 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSHR. Location: chromosome 14, position 81,610,123. Clinical significance in the table: Likely benign.

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Reference-table entries

TSHRLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 14:81610123
Cytoband: 14q31.1
HGVS: NM_000369.5(TSHR):c.1721C>G (p.Thr574Ser)
Allele change: Missense_T574S

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.