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Variant (rsID / SNP)

rs33952257

ACCS

rs33952257 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACCS. Location: chromosome 11, position 44,089,352. The table records no clinical significance for this variant.

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Reference-table entries

ACCSNot classified
Variant type
missense_variant
Chromosome / position
11:44089352
HGVS
NM_001127219.2,c.175G>A,p.Asp59Asn
Allele change
Missense_D59N

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.