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Variant (rsID / SNP)

rs3733560

NDNF

rs3733560 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NDNF. Location: chromosome 4, position 121,958,697. The table records no clinical significance for this variant.

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Reference-table entries

NDNFNot classified
Variant type
synonymous_variant
Chromosome / position
4:121958697
HGVS
NM_024574.4,c.429C>T,p.Ser143Ser
Allele change
Synonymous_S143S

Public references

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