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Variant (rsID / SNP)

rs1190788

AKAP7

rs1190788 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AKAP7. Location: chromosome 6, position 131,520,655. The table records no clinical significance for this variant.

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Reference-table entries

AKAP7Not classified
Variant type
missense_variant
Chromosome / position
6:131520655
HGVS
NM_001376570.1,c.644G>A,p.Ser215Asn
Allele change
Missense_S215N

Public references

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