Variant (rsID / SNP)

rs104893751

rs104893751 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OGG1. Location: chromosome 3, position 9,792,107. Clinical significance in the table: Uncertain significance.

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Reference-table entries

OGG1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 3:9792107
Cytoband: 3p25.3
HGVS: NM_002542.6(OGG1):c.137G>A (p.Arg46Gln)
Allele change: Missense_R46Q

Associated conditions / phenotypes

Clear cell carcinoma of kidney

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.