Variant (rsID / SNP)

rs17014946

rs17014946 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MMAA. Location: chromosome 4, position 146,567,584. Clinical significance in the table: Benign.

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Reference-table entries

MMAABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:146567584
Cytoband: 4q31.21
HGVS: NM_172250.3(MMAA):c.733+276T>G
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.