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Variant (rsID / SNP)

rs45484702

CARMIL3

rs45484702 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CARMIL3. Location: chromosome 14, position 24,526,206. The table records no clinical significance for this variant.

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Reference-table entries

CARMIL3Not classified
Variant type
synonymous_variant
Chromosome / position
14:24526206
HGVS
NM_138360.4,c.1035T>C,p.Pro345Pro
Allele change
Synonymous_P345P

Public references

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