Variant (rsID / SNP)

rs4930729

rs4930729 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH10. Location: chromosome 12, position 124,325,977. Clinical significance in the table: Benign.

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Reference-table entries

DNAH10Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 12:124325977
Cytoband: 12q24.31
HGVS: NM_001372106.1(DNAH10):c.5245T>G (p.Leu1749Val)
Allele change: Missense_L1631V

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.