Variant (rsID / SNP)

rs145970222

rs145970222 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GFM1. Location: chromosome 3, position 158,371,218. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

GFM1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:158371218
Cytoband: 3q25.32
HGVS: NM_024996.7(GFM1):c.960A>C (p.Pro320=)
Allele change: Synonymous_P339P

Associated conditions / phenotypes

Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1

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.