Variant (rsID / SNP)

rs34218846

rs34218846 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IDH1. Location: chromosome 2, position 209,108,317. Clinical significance in the table: Benign.

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Reference-table entries

IDH1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:209108317
Cytoband: 2q34
HGVS: NM_005896.4(IDH1):c.532G>A (p.Val178Ile)
Allele change: Missense_V178I

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.