Variant (rsID / SNP)

rs591157

rs591157 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACSM6. Location: chromosome 10, position 96,954,298. The table records no clinical significance for this variant.

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Reference-table entries

ACSM6Not classified

Variant type: missense_variant
Chromosome / position: 10:96954298
HGVS: NM_207321.3,c.56A>G,p.Glu19Gly
Allele change: Missense_E19G

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.