Variant (rsID / SNP)

rs193922686

rs193922686 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MC4R. Location: chromosome 18, position 58,038,906. Clinical significance in the table: Uncertain significance.

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Reference-table entries

MC4RUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 18:58038906
Cytoband: 18q21.32
HGVS: NM_005912.3(MC4R):c.677T>C (p.Ile226Thr)
Allele change: Missense_I226T

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.