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Variant (rsID / SNP)

rs41271815

CARMIL1

rs41271815 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CARMIL1. Location: chromosome 6, position 25,472,737. The table records no clinical significance for this variant.

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Reference-table entries

CARMIL1Not classified
Variant type
synonymous_variant
Chromosome / position
6:25472737
HGVS
NM_017640.6,c.862C>T,p.Leu288Leu
Allele change
Synonymous_L288L

Public references

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