Variant (rsID / SNP)

rs148490596

rs148490596 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP5F1A. Location: chromosome 18, position 43,678,225. Clinical significance in the table: Benign.

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Reference-table entries

ATP5F1ABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 18:43678225
Cytoband: 18q21.1
HGVS: NM_004046.6(ATP5F1A):c.-28A>G
Allele change: Silent

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.