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Variant (rsID / SNP)

rs1548450

CLEC19A

rs1548450 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLEC19A. Location: chromosome 16, position 19,310,092. The table records no clinical significance for this variant.

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Reference-table entries

CLEC19ANot classified
Variant type
synonymous_variant
Chromosome / position
16:19310092
HGVS
NM_001256720.2,c.186T>C,p.Ala62Ala
Allele change
Synonymous_A62A

Public references

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