Variant (rsID / SNP)

rs13383830

rs13383830 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD207. Location: chromosome 2, position 71,058,306. The table records no clinical significance for this variant.

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Reference-table entries

CD207Not classified

Variant type: missense_variant
Chromosome / position: 2:71058306
HGVS: NM_015717.5,c.862A>G,p.Asn288Asp
Allele change: Missense_N288D

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.