Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs10872670

AKAP12

rs10872670 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AKAP12. Location: chromosome 6, position 151,669,875. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

AKAP12Not classified
Variant type
missense_variant
Chromosome / position
6:151669875
HGVS
NM_005100.4,c.349A>G,p.Lys117Glu
Allele change
Missense_K117E

Public references

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