Variant (rsID / SNP)

rs9678851

rs9678851 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC4A1AP. Location: chromosome 2, position 27,887,034. The table records no clinical significance for this variant.

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Reference-table entries

SLC4A1APNot classified

Variant type: missense_variant
Chromosome / position: 2:27887034
HGVS: NM_018158.3,c.253C>A,p.Pro85Thr
Allele change: Missense_P139T

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.