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Variant (rsID / SNP)

rs11649499

SEZ6L2

rs11649499 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SEZ6L2. Location: chromosome 16, position 29,908,433. The table records no clinical significance for this variant.

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Reference-table entries

SEZ6L2Not classified
Variant type
missense_variant
Chromosome / position
16:29908433
HGVS
NM_001243332.2,c.221G>C,p.Arg74Pro
Allele change
Missense_R74P

Associated conditions / phenotypes

Silent

Public references

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