Variant (rsID / SNP)

rs1277207

rs1277207 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AKNAD1. Location: chromosome 1, position 109,395,105. The table records no clinical significance for this variant.

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Reference-table entries

AKNAD1Not classified

Variant type: missense_variant
Chromosome / position: 1:109395105
HGVS: NM_152763.5,c.182G>A,p.Ser61Asn
Allele change: Missense_S61N

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.