Variant (rsID / SNP)

rs146196839

rs146196839 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DGAT1. Location: chromosome 8, position 145,541,635. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

DGAT1Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 8:145541635
Cytoband: 8q24.3
HGVS: NM_012079.6(DGAT1):c.797A>G (p.Asn266Ser)
Allele change: Missense_N266S

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.