Variant (rsID / SNP)

rs115013548

rs115013548 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RIPOR2. Location: chromosome 6, position 24,843,097. Clinical significance in the table: Benign.

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Reference-table entries

RIPOR2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:24843097
Cytoband: 6p22.3
HGVS: NM_001286445.3(RIPOR2):c.1850T>G (p.Ile617Ser)
Allele change: Missense_I638S

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.