Variant (rsID / SNP)

rs2515960

rs2515960 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NOP14. Location: chromosome 4, position 2,951,804. The table records no clinical significance for this variant.

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Reference-table entries

NOP14Not classified

Variant type: missense_variant
Chromosome / position: 4:2951804
HGVS: NM_001291978.2,c.1139T>C,p.Leu380Ser
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.