Variant (rsID / SNP)
rs77493670
rs77493670 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ICAM4. Location: chromosome 19, position 10,397,987. Clinical significance in the table: Affects.
Reference-table entries
ICAM4Other
- Clinical significance (as recorded)
- Affects
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:10397987
- Cytoband
- 19p13.2
- HGVS
- NM_001544.5(ICAM4):c.299A>G (p.Gln100Arg)
- Allele change
- Missense_Q100R
Associated conditions / phenotypes
Landsteiner-Wiener phenotype
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.