Variant (rsID / SNP)

rs4684677

rs4684677 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GHRL. Location: chromosome 3, position 10,328,453. Clinical significance in the table: Benign.

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Reference-table entries

GHRLBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:10328453
Cytoband: 3p25.3
HGVS: NM_016362.5(GHRL):c.269A>T (p.Gln90Leu)
Allele change: Silent

Associated conditions / phenotypes

Obesity

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.