Variant (rsID / SNP)

rs190788663

rs190788663 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC9A6. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

SLC9A6Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Cytoband: Xq26.3
HGVS: NM_001379110.1(SLC9A6):c.*12C>T
Allele change: Silent

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.