Variant (rsID / SNP)

rs34711402

rs34711402 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AKAP6. Location: chromosome 14, position 33,291,583. The table records no clinical significance for this variant.

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Reference-table entries

AKAP6Not classified

Variant type: missense_variant
Chromosome / position: 14:33291583
HGVS: NM_004274.5,c.4564G>A,p.Val1522Ile
Allele change: Missense_V1522I

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.