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Variant (rsID / SNP)

rs17238540

HMGCR

rs17238540 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HMGCR. Location: chromosome 5, position 74,655,498. Clinical significance in the table: no interpretation for the single variant.

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Reference-table entries

HMGCROther
Clinical significance (as recorded)
no interpretation for the single variant
Variant type
single nucleotide variant
Chromosome / position
5:74655498
Cytoband
5q13.3
HGVS
NM_000859.3(HMGCR):c.2457+117T>G
Allele change
Silent

Associated conditions / phenotypes

Stroke, Ischemic|Coronary Heart Disease 1|Type 2 Diabetes Mellitus|Diabetes Mellitus|Myopathy

Public references

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