Variant (rsID / SNP)

rs3783942

rs3783942 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSHR. Location: chromosome 14, position 81,574,959. The table records no clinical significance for this variant.

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Reference-table entries

TSHRNot classified

Variant type: synonymous_variant
Chromosome / position: 14:81574959
HGVS: NM_001018036.3,c.696A>G,p.Leu232Leu
Allele change: Synonymous_L232L

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.