Variant (rsID / SNP)

rs35277569

rs35277569 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HOXA13. Location: chromosome 7, position 27,239,064. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

HOXA13Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 7:27239064
Cytoband: 7p15.2
HGVS: NM_000522.5(HOXA13):c.633G>T (p.Met211Ile)
Allele change: Missense_M211I

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.