Variant (rsID / SNP)

rs34911341

rs34911341 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GHRL. Location: chromosome 3, position 10,331,519. Clinical significance in the table: risk factor.

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Reference-table entries

GHRLRisk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 3:10331519
Cytoband: 3p25.3
HGVS: NM_016362.5(GHRL):c.152G>A (p.Arg51Gln)
Allele change: Silent

Associated conditions / phenotypes

Metabolic syndrome, susceptibility to|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.