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Variant (rsID / SNP)

rs2295322

CHMP4A

rs2295322 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CHMP4A. Location: chromosome 14, position 24,679,877. The table records no clinical significance for this variant.

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Reference-table entries

CHMP4ANot classified
Variant type
missense_variant
Chromosome / position
14:24679877
HGVS
NM_014169.5,c.457G>A,p.Gly153Arg
Allele change
Missense_G196R

Public references

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