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Variant (rsID / SNP)

rs1043620

HSPA1A

rs1043620 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HSPA1A. Location: chromosome 6, position 31,783,755. The table records no clinical significance for this variant.

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Reference-table entries

HSPA1ANot classified
Variant type
synonymous_variant
Chromosome / position
6:31783755
HGVS
NM_005345.6,c.222T>C,p.Ile74Ile
Allele change
Synonymous_I74I

Public references

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