Variant (rsID / SNP)

rs137882374

rs137882374 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GH1. Location: chromosome 17, position 61,995,213. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

GH1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:61995213
Cytoband: 17q23.3
HGVS: NM_000515.5(GH1):c.363T>A (p.Ser121Arg)
Allele change: Missense_S121R

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.