Variant (rsID / SNP)
rs11276
rs11276 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ART4. Location: chromosome 12, position 14,993,439. Clinical significance in the table: Affects.
Reference-table entries
ART4Other
- Clinical significance (as recorded)
- Affects
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:14993439
- Cytoband
- 12p12.3
- HGVS
- NM_021071.4(ART4):c.793G>A (p.Asp265Asn)
- Allele change
- Missense_D265N
Associated conditions / phenotypes
Blood group, Dombrock system
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.