Variant (rsID / SNP)

rs6763202

rs6763202 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC9A9. Location: chromosome 3, position 143,293,012. Clinical significance in the table: Benign.

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Reference-table entries

SLC9A9Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:143293012
Cytoband: 3q24
HGVS: NM_173653.4(SLC9A9):c.918T>C (p.Cys306=)
Allele change: Synonymous_C306C

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.