Variant (rsID / SNP)

rs2277398

rs2277398 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANO2. Location: chromosome 12, position 5,674,754. The table records no clinical significance for this variant.

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Reference-table entries

ANO2Not classified

Variant type: synonymous_variant
Chromosome / position: 12:5674754
HGVS: NM_001278596.3,c.2712C>T,p.Ser904Ser
Allele change: Synonymous_S900S

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.