Variant (rsID / SNP)

rs121913556

rs121913556 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MC3R. Location: chromosome 20, position 54,824,792. Clinical significance in the table: risk factor.

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Reference-table entries

MC3RRisk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 20:54824792
Cytoband: 20q13.2
HGVS: NM_019888.3(MC3R):c.893T>G (p.Ile298Ser)
Allele change: Missense_I298S

Associated conditions / phenotypes

Body mass index quantitative trait locus 9

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.