Variant (rsID / SNP)
rs1042034
rs1042034 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOB. Location: chromosome 2, position 21,225,281. Clinical significance in the table: Benign.
Reference-table entries
APOBBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- missense_variant
- Chromosome / position
- 2:21225281
- HGVS
- NM_000384.3,c.13013G>A,p.Ser4338Asn
- Allele change
- Missense_S4338N
Associated conditions / phenotypes
Lipid Metabolism Disorder|Type 2 Diabetes Mellitus|Kidney Disease|Hepatitis C|Hepatitis C Virus|Hepatitis|Osteonecrosis|Stroke, Ischemic|Avascular Necrosis of Femoral Head, Primary, 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.