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Variant (rsID / SNP)

rs1545437

FREM3

rs1545437 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FREM3. Location: chromosome 4, position 144,617,842. The table records no clinical significance for this variant.

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Reference-table entries

FREM3Not classified
Variant type
synonymous_variant
Chromosome / position
4:144617842
HGVS
NM_001168235.2,c.3987C>A,p.Ile1329Ile
Allele change
Synonymous_I1329I

Public references

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