Variant (rsID / SNP)

rs11084024

rs11084024 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLEC11A. Location: chromosome 19, position 51,228,634. The table records no clinical significance for this variant.

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Reference-table entries

CLEC11ANot classified

Variant type: synonymous_variant
Chromosome / position: 19:51228634
HGVS: NM_002975.3,c.882G>A,p.Glu294Glu
Allele change: Synonymous_E294E

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.