Variant (rsID / SNP)

rs857691

rs857691 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPTA1. Location: chromosome 1, position 158,626,378. Clinical significance in the table: Benign.

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Reference-table entries

SPTA1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:158626378
Cytoband: 1q23.1
HGVS: NM_003126.4(SPTA1):c.2874G>A (p.Leu958=)
Allele change: Synonymous_L958L

Associated conditions / phenotypes

Hereditary spherocytosis type 3|Elliptocytosis 2|Pyropoikilocytosis, hereditary

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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