Variant (rsID / SNP)

rs608052

rs608052 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRMT9B. Location: chromosome 8, position 12,879,539. The table records no clinical significance for this variant.

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Reference-table entries

TRMT9BNot classified

Variant type: missense_variant
Chromosome / position: 8:12879539
HGVS: NM_020844.3,c.1351A>G,p.Arg451Gly
Allele change: Missense_R451G

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.