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Variant (rsID / SNP)

rs2394656

AIFM2

rs2394656 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AIFM2. Location: chromosome 10, position 71,876,382. The table records no clinical significance for this variant.

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Reference-table entries

AIFM2Not classified
Variant type
synonymous_variant
Chromosome / position
10:71876382
HGVS
NM_001198696.2,c.765G>A,p.Ala255Ala
Allele change
Synonymous_A255A

Public references

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