Variant (rsID / SNP)

rs201351567

rs201351567 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC4A10. Location: chromosome 2, position 162,805,760. Clinical significance in the table: Uncertain significance.

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Reference-table entries

SLC4A10Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 2:162805760
Cytoband: 2q24.2
HGVS: NM_001178015.2(SLC4A10):c.2368A>G (p.Ser790Gly)
Allele change: Missense_S790G

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.