Variant (rsID / SNP)

rs188461284

rs188461284 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MTFMT. Location: chromosome 15, position 65,312,589. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

MTFMTBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 15:65312589
Cytoband: 15q22.31
HGVS: NM_139242.4(MTFMT):c.667T>A (p.Leu223Met)
Allele change: Missense_L223M

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.