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Variant (rsID / SNP)

rs41282288

NXT1

rs41282288 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NXT1. Location: chromosome 20, position 23,334,781. The table records no clinical significance for this variant.

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Reference-table entries

NXT1Not classified
Variant type
synonymous_variant
Chromosome / position
20:23334781
HGVS
NM_013248.3,c.103C>T,p.Leu35Leu
Allele change
Synonymous_L35L

Public references

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