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Variant (rsID / SNP)

rs4851287

LONRF2

rs4851287 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LONRF2. Location: chromosome 2, position 100,915,772. The table records no clinical significance for this variant.

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Reference-table entries

LONRF2Not classified
Variant type
missense_variant
Chromosome / position
2:100915772
HGVS
NM_198461.4,c.1277T>C,p.Leu426Pro
Allele change
Missense_L426P

Public references

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