Variant (rsID / SNP)

rs33935373

rs33935373 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH10. Location: chromosome 12, position 124,337,772. 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: 12:124337772
Cytoband: 12q24.31
HGVS: NM_001372106.1(DNAH10):c.6311C>T (p.Thr2104Met)
Allele change: Missense_T1986M

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.