Variant (rsID / SNP)

rs4720015

rs4720015 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to INMT. Location: chromosome 7, position 30,795,436. The table records no clinical significance for this variant.

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Reference-table entries

INMTNot classified

Variant type: missense_variant
Chromosome / position: 7:30795436
HGVS: NM_006774.5,c.761T>G,p.Phe254Cys
Allele change: Silent

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.