Variant (rsID / SNP)
rs74315393
rs74315393 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MC3R. Location: chromosome 20, position 54,824,336. Clinical significance in the table: risk factor.
Reference-table entries
MC3RRisk factor
- Clinical significance (as recorded)
- risk factor
- Variant type
- single nucleotide variant
- Chromosome / position
- 20:54824336
- Cytoband
- 20q13.2
- HGVS
- NM_019888.3(MC3R):c.437T>A (p.Ile146Asn)
- Allele change
- Missense_I146N
Associated conditions / phenotypes
Body mass index quantitative trait locus 9
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.