Variant (rsID / SNP)

rs55756985

rs55756985 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NXF5. The table records no clinical significance for this variant.

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Reference-table entries

NXF5Not classified

Variant type: intron_variant
HGVS: NR_159736.1,n.412-400A>G
Allele change: Missense_K23E

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.