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Variant (rsID / SNP)

rs201265160

SLC4A1

rs201265160 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC4A1. Location: chromosome 17, position 42,327,861. 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
17:42327861
Cytoband
17q21.31
HGVS
NM_000342.4(SLC4A1):c.2701C>T (p.Arg901Trp)
Allele change
Missense_R901W

Associated conditions / phenotypes

Hereditary spherocytosis type 4|Hemolytic anemia|Autosomal dominant distal renal tubular acidosis

Public references

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