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Variant (rsID / SNP)

rs4853018

SLC4A5

rs4853018 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC4A5. Location: chromosome 2, position 74,466,594. The table records no clinical significance for this variant.

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Reference-table entries

SLC4A5Not classified
Variant type
synonymous_variant
Chromosome / position
2:74466594
HGVS
NM_021196.3,c.2187C>T,p.Gly729Gly
Allele change
Synonymous_G729G

Public references

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