Variant (rsID / SNP)

rs2822787

rs2822787 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SAMSN1. Location: chromosome 21, position 15,954,660. The table records no clinical significance for this variant.

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Reference-table entries

SAMSN1Not classified

Variant type: missense_variant
Chromosome / position: 21:15954660
HGVS: NM_001395858.1,c.838A>G,p.Asn280Asp
Allele change: Missense_N20D

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.