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Variant (rsID / SNP)

rs12201388

AKAP12

rs12201388 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AKAP12. Location: chromosome 6, position 151,673,589. The table records no clinical significance for this variant.

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Reference-table entries

AKAP12Not classified
Variant type
missense_variant
Chromosome / position
6:151673589
HGVS
NM_005100.4,c.4063G>A,p.Glu1355Lys
Allele change
Missense_E1355K

Public references

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