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Variant (rsID / SNP)

rs4296198

FAM81A

rs4296198 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM81A. Location: chromosome 15, position 59,784,493. The table records no clinical significance for this variant.

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Reference-table entries

FAM81ANot classified
Variant type
synonymous_variant
Chromosome / position
15:59784493
HGVS
NM_152450.3,c.318C>T,p.Ala106Ala
Allele change
Synonymous_A106A

Public references

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