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Variant (rsID / SNP)

rs1488988

SPAG16

rs1488988 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPAG16. Location: chromosome 2, position 214,161,849. The table records no clinical significance for this variant.

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Reference-table entries

SPAG16Not classified
Variant type
intron_variant
Chromosome / position
2:214161849
HGVS
NM_024532.5,c.184-137C>T
Allele change
Silent

Public references

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