Variant (rsID / SNP)

rs314378

rs314378 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC12A9. Location: chromosome 7, position 100,458,795. The table records no clinical significance for this variant.

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Reference-table entries

SLC12A9Not classified

Variant type: synonymous_variant
Chromosome / position: 7:100458795
HGVS: NM_001363493.2,c.1254T>C,p.Ala418Ala
Allele change: Synonymous_A275A

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.