Variant (rsID / SNP)

rs41302817

rs41302817 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HMGCS2. Location: chromosome 1, position 120,307,084. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

HMGCS2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:120307084
Cytoband: 1p12
HGVS: NM_005518.4(HMGCS2):c.270G>A (p.Gln90=)
Allele change: Synonymous_Q90Q

Associated conditions / phenotypes

3-hydroxy-3-methylglutaryl-CoA synthase deficiency

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.