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Variant (rsID / SNP)

rs10456324

CARMIL1

rs10456324 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CARMIL1. Location: chromosome 6, position 25,600,968. The table records no clinical significance for this variant.

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Reference-table entries

CARMIL1Not classified
Variant type
synonymous_variant
Chromosome / position
6:25600968
HGVS
NM_017640.6,c.3546G>A,p.Ala1182Ala
Allele change
Synonymous_A1182A

Public references

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