Variant (rsID / SNP)

rs61421370

rs61421370 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AHNAK2. Location: chromosome 14, position 105,406,372. The table records no clinical significance for this variant.

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Reference-table entries

AHNAK2Not classified

Variant type: missense_variant
Chromosome / position: 14:105406372
HGVS: NM_138420.4,c.15416G>A,p.Gly5139Glu
Allele change: Missense_G5139E

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.