Variant (rsID / SNP)

rs3748597

rs3748597 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NOC2L. Location: chromosome 1, position 888,659. The table records no clinical significance for this variant.

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Reference-table entries

NOC2LNot classified

Variant type: missense_variant
Chromosome / position: 1:888659
HGVS: NM_015658.4,c.898A>G,p.Ile300Val
Allele change: Missense_I300V

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.