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Variant (rsID / SNP)

rs3094134

TRIM10

rs3094134 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIM10. Location: chromosome 6, position 30,122,154. The table records no clinical significance for this variant.

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Reference-table entries

TRIM10Not classified
Variant type
synonymous_variant
Chromosome / position
6:30122154
HGVS
NM_006778.4,c.1038A>G,p.Gln346Gln
Allele change
Synonymous_Q346Q

Public references

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