Variant (rsID / SNP)
rs7213894
rs7213894 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH2. Location: chromosome 17, position 7,722,365. Clinical significance in the table: Benign.
Reference-table entries
DNAH2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:7722365
- Cytoband
- 17p13.1
- HGVS
- NM_020877.5(DNAH2):c.10799C>T (p.Thr3600Ile)
- Allele change
- Missense_T3600I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.