Variant (rsID / SNP)

rs41293277

rs41293277 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NSUN4. Location: chromosome 1, position 46,806,550. The table records no clinical significance for this variant.

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Reference-table entries

NSUN4Not classified

Variant type: missense_variant
Chromosome / position: 1:46806550
HGVS: NM_199044.4,c.52C>T,p.Leu18Phe
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.