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Variant (rsID / SNP)

rs2075799

HSPA1L

rs2075799 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HSPA1L. Location: chromosome 6, position 31,778,529. The table records no clinical significance for this variant.

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Reference-table entries

HSPA1LNot classified
Variant type
synonymous_variant
Chromosome / position
6:31778529
HGVS
NM_005527.4,c.1221G>A,p.Thr407Thr
Allele change
Synonymous_T407T

Associated conditions / phenotypes

Schizophrenia|Systemic Lupus Erythematosus|Major Affective Disorder 8|Major Affective Disorder 9|Lupus Erythematosus|Bipolar Disorder

Public references

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