Variant (rsID / SNP)

rs149278617

rs149278617 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC25A12. Location: chromosome 2, position 172,650,245. 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: 2:172650245
Cytoband: 2q31.1
HGVS: NM_003705.5(SLC25A12):c.1338A>C (p.Pro446=)
Allele change: Synonymous_P446P

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.