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Variant (rsID / SNP)

rs12623569

SPAG16

rs12623569 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPAG16. Location: chromosome 2, position 214,794,743. The table records no clinical significance for this variant.

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Reference-table entries

SPAG16Not classified
Variant type
missense_variant
Chromosome / position
2:214794743
HGVS
NM_024532.5,c.1274A>C,p.Lys425Thr
Allele change
Missense_K425T

Public references

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