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Variant (rsID / SNP)

rs2001301

LRRFIP1

rs2001301 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRRFIP1. Location: chromosome 2, position 238,671,609. The table records no clinical significance for this variant.

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Reference-table entries

LRRFIP1Not classified
Variant type
missense_variant
Chromosome / position
2:238671609
HGVS
NM_001137552.2,c.1253A>G,p.Asn418Ser
Allele change
Silent

Public references

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