Variant (rsID / SNP)

rs55907012

rs55907012 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DGAT1. Location: chromosome 8, position 145,542,375. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

DGAT1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 8:145542375
Cytoband: 8q24.3
HGVS: NM_012079.6(DGAT1):c.455A>G (p.Lys152Arg)
Allele change: Missense_K152R

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.