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Variant (rsID / SNP)

rs2023472

TRIM31

rs2023472 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIM31. Location: chromosome 6, position 30,075,864. The table records no clinical significance for this variant.

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Reference-table entries

TRIM31Not classified
Variant type
synonymous_variant
Chromosome / position
6:30075864
HGVS
NM_007028.5,c.849T>C,p.His283His
Allele change
Synonymous_H283H

Public references

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