Variant (rsID / SNP)

rs75558206

rs75558206 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH10. Location: chromosome 12, position 124,387,669. 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: 12:124387669
Cytoband: 12q24.31
HGVS: NM_001372106.1(DNAH10):c.9815+9C>T
Allele change: Silent

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.