Variant (rsID / SNP)

rs35331811

rs35331811 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RIPOR2. Location: chromosome 6, position 24,848,372. 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: 6:24848372
Cytoband: 6p22.3
HGVS: NM_001286445.3(RIPOR2):c.1045G>A (p.Val349Met)
Allele change: Missense_V320M

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.