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Variant (rsID / SNP)

rs9371533

RAET1E

rs9371533 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAET1E. Location: chromosome 6, position 150,210,681. The table records no clinical significance for this variant.

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Reference-table entries

RAET1ENot classified
Variant type
missense_variant
Chromosome / position
6:150210681
HGVS
NM_001394057.1,c.425C>T,p.Thr142Ile
Allele change
Silent

Associated conditions / phenotypes

Lipoprotein Quantitative Trait Locus|Arteries, Anomalies of

Public references

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