Variant (rsID / SNP)

rs3742926

rs3742926 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AKAP6. Location: chromosome 14, position 33,014,869. The table records no clinical significance for this variant.

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Reference-table entries

AKAP6Not classified

Variant type: missense_variant
Chromosome / position: 14:33014869
HGVS: NM_004274.5,c.1010C>T,p.Ala337Val
Allele change: Missense_A337V

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.