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Variant (rsID / SNP)

rs17049006

TRAM1L1

rs17049006 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRAM1L1. Location: chromosome 4, position 118,006,307. The table records no clinical significance for this variant.

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Reference-table entries

TRAM1L1Not classified
Variant type
synonymous_variant
Chromosome / position
4:118006307
HGVS
NM_152402.3,c.243C>T,p.Ala81Ala
Allele change
Synonymous_A81A

Public references

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