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Variant (rsID / SNP)

rs13212161

AKAP12

rs13212161 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AKAP12. Location: chromosome 6, position 151,672,285. The table records no clinical significance for this variant.

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Reference-table entries

AKAP12Not classified
Variant type
missense_variant
Chromosome / position
6:151672285
HGVS
NM_005100.4,c.2759A>G,p.Glu920Gly
Allele change
Missense_E920G

Public references

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