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Variant (rsID / SNP)

rs3738413

TRIM45

rs3738413 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIM45. Location: chromosome 1, position 117,659,352. The table records no clinical significance for this variant.

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Reference-table entries

TRIM45Not classified
Variant type
missense_variant
Chromosome / position
1:117659352
HGVS
NM_025188.4,c.1238G>A,p.Arg413Gln
Allele change
Missense_R413Q

Public references

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