Variant (rsID / SNP)

rs2680903

rs2680903 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NSMAF. Location: chromosome 8, position 59,512,334. The table records no clinical significance for this variant.

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Reference-table entries

NSMAFNot classified

Variant type: synonymous_variant
Chromosome / position: 8:59512334
HGVS: NM_001144772.1,c.1521C>T,p.Asp507Asp
Allele change: Synonymous_D476D

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.