Variant (rsID / SNP)

rs2832

rs2832 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SUCLG1. Location: chromosome 2, position 84,650,707. Clinical significance in the table: Benign.

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Reference-table entries

SUCLG1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:84650707
Cytoband: 2p11.2
HGVS: NM_003849.4(SUCLG1):c.*163T>C
Allele change: Silent

Associated conditions / phenotypes

Mitochondrial DNA depletion syndrome 9|Mitochondrial DNA depletion syndrome

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.