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Variant (rsID / SNP)

rs11230563

CD6

rs11230563 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD6. Location: chromosome 11, position 60,776,209. The table records no clinical significance for this variant.

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Reference-table entries

CD6Not classified
Variant type
missense_variant
Chromosome / position
11:60776209
HGVS
NM_006725.5,c.673C>T,p.Arg225Trp
Allele change
Silent

Associated conditions / phenotypes

Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity|Skin Disease|Pustulosis of Palm and Sole|Psoriasis|Cerebrofacial Arteriovenous Metameric Syndrome

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.