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Variant (rsID / SNP)

rs11264580

PEAR1

rs11264580 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PEAR1. Location: chromosome 1, position 156,878,531. The table records no clinical significance for this variant.

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Reference-table entries

PEAR1Not classified
Variant type
synonymous_variant
Chromosome / position
1:156878531
HGVS
NM_001080471.3,c.1200T>C,p.His400His
Allele change
Synonymous_H336H

Associated conditions / phenotypes

Coronary Heart Disease 1|Ischemia

Public references

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