Variant (rsID / SNP)

rs1880024

rs1880024 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRMT44. Location: chromosome 4, position 8,454,639. The table records no clinical significance for this variant.

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Reference-table entries

TRMT44Not classified

Variant type: missense_variant
Chromosome / position: 4:8454639
HGVS: NM_152544.3,c.1054A>G,p.Arg352Gly
Allele change: Missense_R111G

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.