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Variant (rsID / SNP)

rs1210894

SEZ6L

rs1210894 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SEZ6L. Location: chromosome 22, position 26,702,015. The table records no clinical significance for this variant.

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Reference-table entries

SEZ6LNot classified
Variant type
synonymous_variant
Chromosome / position
22:26702015
HGVS
NM_021115.5,c.1419A>C,p.Thr473Thr
Allele change
Synonymous_T473T

Associated conditions / phenotypes

Synonymous_T473T

Public references

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