Variant (rsID / SNP)

rs61740106

rs61740106 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRH. Location: chromosome 3, position 129,695,578. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

TRHBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:129695578
Cytoband: 3q22.1
HGVS: NM_007117.5(TRH):c.248G>A (p.Arg83His)
Allele change: Missense_R83H

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.