Variant (rsID / SNP)

rs2242637

rs2242637 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARTN. Location: chromosome 1, position 44,401,384. The table records no clinical significance for this variant.

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Reference-table entries

ARTNNot classified

Variant type: missense_variant
Chromosome / position: 1:44401384
HGVS: NM_001136215.2,c.56A>G,p.Gln19Arg
Allele change: Missense_Q19R

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.