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Variant (rsID / SNP)

rs4693

NXF1

rs4693 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NXF1. Location: chromosome 11, position 62,564,009. The table records no clinical significance for this variant.

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Reference-table entries

NXF1Not classified
Variant type
synonymous_variant
Chromosome / position
11:62564009
HGVS
NM_006362.5,c.1209A>G,p.Arg403Arg
Allele change
Silent

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.