Variant (rsID / SNP)

rs10495237

rs10495237 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH14. Location: chromosome 1, position 225,506,294. Clinical significance in the table: Benign.

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Reference-table entries

DNAH14Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:225506294
Cytoband: 1q42.12
HGVS: NM_001367479.1(DNAH14):c.9250A>G (p.Asn3084Asp)
Allele change: Missense_N2991D

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.