Variant (rsID / SNP)
rs62001448
rs62001448 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TYRO3. Location: chromosome 15, position 41,865,525. Clinical significance in the table: Benign.
Reference-table entries
TYRO3Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- missense_variant
- Chromosome / position
- 15:41865525
- HGVS
- NM_006293.4,c.2005G>T,p.Val669Leu
- Allele change
- Missense_V669L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.