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Variant (rsID / SNP)

rs4664114

FMNL2

rs4664114 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FMNL2. Location: chromosome 2, position 153,378,459. The table records no clinical significance for this variant.

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Reference-table entries

FMNL2Not classified
Variant type
splice_region_variant&synonymous_variant
Chromosome / position
2:153378459
HGVS
NM_052905.4,c.120T>C,p.Asn40Asn
Allele change
Synonymous_N40N

Public references

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