Variant (rsID / SNP)

rs555136684

rs555136684 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HOXD13. Location: chromosome 2, position 176,957,659. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

HOXD13Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 2:176957659
Cytoband: 2q31.1
HGVS: NM_000523.4(HOXD13):c.41C>T (p.Ala14Val)
Allele change: Missense_A14V

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.