Variant (rsID / SNP)

rs35413309

rs35413309 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RGS9BP, ANKRD27. Location: chromosome 19, position 33,167,837. Clinical significance in the table: Benign.

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Reference-table entries

RGS9BPBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:33167837
Cytoband: 19q13.11
HGVS: NM_207391.3(RGS9BP):c.668C>T (p.Ala223Val)
Allele change: Missense_A223V

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.