Variant (rsID / SNP)

rs144160937

rs144160937 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HOXD10. Location: chromosome 2, position 176,983,934. Clinical significance in the table: Benign.

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Reference-table entries

HOXD10Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:176983934
Cytoband: 2q31.1
HGVS: NM_002148.4(HOXD10):c.998T>C (p.Leu333Pro)
Allele change: Missense_L333P

Associated conditions / phenotypes

Congenital vertical talus

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.