Variant (rsID / SNP)

rs35565687

rs35565687 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC25A12. Location: chromosome 2, position 172,650,165. 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: 2:172650165
Cytoband: 2q31.1
HGVS: NM_003705.5(SLC25A12):c.1418G>A (p.Arg473Gln)
Allele change: Missense_R473Q

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.