Variant (rsID / SNP)

rs722896

rs722896 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLEC4F. Location: chromosome 2, position 71,043,461. The table records no clinical significance for this variant.

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Reference-table entries

CLEC4FNot classified

Variant type: missense_variant
Chromosome / position: 2:71043461
HGVS: NM_173535.3,c.1052G>A,p.Arg351His
Allele change: Missense_R351H

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.