Variant (rsID / SNP)

rs2275462

rs2275462 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIM9. Location: chromosome 14, position 51,446,216. The table records no clinical significance for this variant.

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Reference-table entries

TRIM9Not classified

Variant type: missense_variant
Chromosome / position: 14:51446216
HGVS: NM_001387360.1,c.2214A>C,p.Leu738Phe
Allele change: Missense_L653F

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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