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Variant (rsID / SNP)

rs289834

NMI

rs289834 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NMI. Location: chromosome 2, position 152,132,130. The table records no clinical significance for this variant.

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Reference-table entries

NMINot classified
Variant type
synonymous_variant
Chromosome / position
2:152132130
HGVS
NM_004688.3,c.502T>C,p.Leu168Leu
Allele change
Synonymous_L168L

Public references

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