Variant (rsID / SNP)

rs7959451

rs7959451 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLEC7A. Location: chromosome 12, position 10,271,055. Clinical significance in the table: Benign.

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Reference-table entries

CLEC7ABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 12:10271055
Cytoband: 12p13.2
HGVS: NM_197947.3(CLEC7A):c.*2A>G
Allele change: Silent

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.