Variant (rsID / SNP)

rs11714448

rs11714448 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC12A8. Location: chromosome 3, position 124,829,057. The table records no clinical significance for this variant.

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Reference-table entries

SLC12A8Not classified

Variant type: synonymous_variant
Chromosome / position: 3:124829057
HGVS: NM_001195483.2,c.1035T>C,p.Pro345Pro
Allele change: Synonymous_P345P

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.