Variant (rsID / SNP)

rs42318

rs42318 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LENG1, CNOT3. Location: chromosome 19, position 54,657,069. The table records no clinical significance for this variant.

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Reference-table entries

LENG1Not classified

Variant type: downstream_gene_variant
Chromosome / position: 19:54657069
HGVS: NM_024316.3,c.*2390G>A
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.