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Variant (rsID / SNP)

rs4878588

FAM205A

rs4878588 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM205A. Location: chromosome 9, position 34,723,744. The table records no clinical significance for this variant.

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Reference-table entries

FAM205ANot classified
Variant type
missense_variant
Chromosome / position
9:34723744
HGVS
NM_001141917.2,c.3493G>T,p.Ala1165Ser
Allele change
Missense_A1165S

Public references

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