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Variant (rsID / SNP)

rs6537825

TRIM33

rs6537825 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIM33. Location: chromosome 1, position 114,948,281. The table records no clinical significance for this variant.

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Reference-table entries

TRIM33Not classified
Variant type
missense_variant
Chromosome / position
1:114948281
HGVS
NM_015906.4,c.2519T>C,p.Ile840Thr
Allele change
Missense_I840T

Public references

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