Variant (rsID / SNP)

rs5983003

rs5983003 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARSF. The table records no clinical significance for this variant.

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Reference-table entries

ARSFNot classified

Variant type: synonymous_variant
HGVS: NM_001201538.2,c.810A>G,p.Glu270Glu
Allele change: Synonymous_E270E

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.