Variant (rsID / SNP)

rs2946655

rs2946655 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MTFMT. Location: chromosome 15, position 65,321,938. Clinical significance in the table: Benign.

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Reference-table entries

MTFMTBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 15:65321938
Cytoband: 15q22.31
HGVS: NM_139242.4(MTFMT):c.14T>C (p.Val5Ala)
Allele change: Missense_V5A

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.