Variant (rsID / SNP)

rs17825620

rs17825620 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SNW1. Location: chromosome 14, position 78,184,661. The table records no clinical significance for this variant.

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Reference-table entries

SNW1Not classified

Variant type: missense_variant
Chromosome / position: 14:78184661
HGVS: NM_001318844.2,c.1461A>C,p.Lys487Asn
Allele change: Missense_K487N

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.