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Variant (rsID / SNP)

rs7947230

TRIM66

rs7947230 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIM66. Location: chromosome 11, position 8,646,670. The table records no clinical significance for this variant.

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Reference-table entries

TRIM66Not classified
Variant type
missense_variant
Chromosome / position
11:8646670
HGVS
NM_001388022.1,c.2416A>C,p.Asn806His
Allele change
Missense_N661H

Public references

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