Variant (rsID / SNP)

rs4946206

rs4946206 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RFX6. Location: chromosome 6, position 117,246,719. Clinical significance in the table: Benign.

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Reference-table entries

RFX6Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:117246719
Cytoband: 6q22.1
HGVS: NM_173560.4(RFX6):c.1782C>T (p.His594=)
Allele change: Synonymous_H594H

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.