Variant (rsID / SNP)

rs2241268

rs2241268 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AKAP13. Location: chromosome 15, position 86,278,309. The table records no clinical significance for this variant.

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Reference-table entries

AKAP13Not classified

Variant type: missense_variant
Chromosome / position: 15:86278309
HGVS: NM_006738.6,c.7381G>A,p.Gly2461Ser
Allele change: Missense_G2457S

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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