Variant (rsID / SNP)

rs1045686

rs1045686 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NAP1L3. The table records no clinical significance for this variant.

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Reference-table entries

NAP1L3Not classified

Variant type: missense_variant
HGVS: NM_004538.6,c.670C>G,p.Pro224Ala
Allele change: Missense_P224A

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.