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Variant (rsID / SNP)

rs1453458

SLC4A4

rs1453458 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC4A4. Location: chromosome 4, position 72,425,863. The table records no clinical significance for this variant.

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Reference-table entries

SLC4A4Not classified
Variant type
synonymous_variant
Chromosome / position
4:72425863
HGVS
NM_001134742.2,c.2991C>T,p.His997His
Allele change
Synonymous_H997H

Public references

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