Variant (rsID / SNP)

rs79199039

rs79199039 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MBOAT7. Location: chromosome 19, position 54,677,793. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

MBOAT7Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 19:54677793
Cytoband: 19q13.42
HGVS: NM_024298.5(MBOAT7):c.1364G>A (p.Arg455Gln)
Allele change: Missense_R455Q

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.