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Variant (rsID / SNP)

rs2293536

UTRN

rs2293536 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UTRN. Location: chromosome 6, position 144,878,337. The table records no clinical significance for this variant.

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Reference-table entries

UTRNNot classified
Variant type
synonymous_variant
Chromosome / position
6:144878337
HGVS
NM_007124.3,c.7179G>T,p.Ala2393Ala
Allele change
Synonymous_A2393A

Public references

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