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Variant (rsID / SNP)

rs7917

NIF3L1

rs7917 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NIF3L1. Location: chromosome 2, position 201,768,238. The table records no clinical significance for this variant.

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Reference-table entries

NIF3L1Not classified
Variant type
missense_variant
Chromosome / position
2:201768238
HGVS
NM_001136039.2,c.971C>T,p.Thr324Ile
Allele change
Missense_T324I

Public references

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