Variant (rsID / SNP)

rs13009279

rs13009279 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TOGARAM2. Location: chromosome 2, position 29,222,070. The table records no clinical significance for this variant.

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Reference-table entries

TOGARAM2Not classified

Variant type: missense_variant
Chromosome / position: 2:29222070
HGVS: NM_199280.4,c.163G>A,p.Ala55Thr
Allele change: Missense_A55T

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.