Variant (rsID / SNP)

rs35881803

rs35881803 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC25A12. Location: chromosome 2, position 172,691,260. Clinical significance in the table: Benign.

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Reference-table entries

SLC25A12Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:172691260
Cytoband: 2q31.1
HGVS: NM_003705.5(SLC25A12):c.728G>A (p.Arg243Lys)
Allele change: Missense_R243K

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.