Variant (rsID / SNP)

rs2272022

rs2272022 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD200. Location: chromosome 3, position 112,063,850. The table records no clinical significance for this variant.

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Reference-table entries

CD200Not classified

Variant type: missense_variant
Chromosome / position: 3:112063850
HGVS: NM_001004196.4,c.211C>A,p.Pro71Thr
Allele change: Missense_P46T

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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