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Variant (rsID / SNP)

rs28931583

SLC4A1

rs28931583 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC4A1. Location: chromosome 17, position 42,335,888. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

SLC4A1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
17:42335888
Cytoband
17q21.31
HGVS
NM_000342.3(SLC4A1):c.980C>G (p.Pro327Arg)
Allele change
Missense_P327R

Associated conditions / phenotypes

Hereditary spherocytosis type 4

Public references

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