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Variant (rsID / SNP)

rs121913561

MC4R

rs121913561 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MC4R. Location: chromosome 18, position 58,038,762. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

MC4RConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
18:58038762
Cytoband
18q21.32
HGVS
NM_005912.3(MC4R):c.821A>G (p.Asn274Ser)
Allele change
Missense_N274S

Associated conditions / phenotypes

BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 20|Obesity

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.