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Variant (rsID / SNP)

rs7285694

AIFM3

rs7285694 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AIFM3. Location: chromosome 22, position 21,330,787. The table records no clinical significance for this variant.

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Reference-table entries

AIFM3Not classified
Variant type
synonymous_variant
Chromosome / position
22:21330787
HGVS
NM_001386814.1,c.990C>T,p.Ala330Ala
Allele change
Synonymous_A330A

Public references

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