Variant (rsID / SNP)

rs62227165

rs62227165 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SAMSN1. Location: chromosome 21, position 15,873,026. The table records no clinical significance for this variant.

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Reference-table entries

SAMSN1Not classified

Variant type: missense_variant
Chromosome / position: 21:15873026
HGVS: NM_001395858.1,c.1576A>G,p.Thr526Ala
Allele change: Missense_T266A

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.