Variant (rsID / SNP)

rs6860077

rs6860077 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC4A9. Location: chromosome 5, position 139,745,154. The table records no clinical significance for this variant.

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Reference-table entries

SLC4A9Not classified

Variant type: splice_region_variant&synonymous_variant
Chromosome / position: 5:139745154
HGVS: NM_001258426.2,c.1668T>C,p.Ile556Ile
Allele change: Synonymous_I567I

Associated conditions / phenotypes

Chiari Malformation Type I|Chiari Malformation

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.