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Variant (rsID / SNP)

rs60858447

HSPA12B

rs60858447 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HSPA12B. Location: chromosome 20, position 3,732,225. The table records no clinical significance for this variant.

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Reference-table entries

HSPA12BNot classified
Variant type
synonymous_variant
Chromosome / position
20:3732225
HGVS
NM_052970.5,c.1473G>A,p.Glu491Glu
Allele change
Synonymous_E490E

Public references

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