Variant (rsID / SNP)

rs6773138

rs6773138 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC12A8. Location: chromosome 3, position 124,826,408. The table records no clinical significance for this variant.

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Reference-table entries

SLC12A8Not classified

Variant type: missense_variant
Chromosome / position: 3:124826408
HGVS: NM_001195483.2,c.1622A>G,p.Lys541Arg
Allele change: Missense_K541R

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.