Variant (rsID / SNP)
rs1801132
rs1801132 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ESR1. Location: chromosome 6, position 152,265,522. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- synonymous_variant
- Chromosome / position
- 6:152265522
- HGVS
- NM_001291230.2,c.981G>C,p.Pro327Pro
- Allele change
- Synonymous_P325P
Associated conditions / phenotypes
Migraine with or Without Aura 1|Migraine with Aura|Gallbladder Disease 1|Breast Cancer|Gallbladder Cancer|Migraine Without Aura|Hypercholesterolemia, Familial, 1|Alzheimer Disease|Mammographic Density|Hypercholesterolemia, Familial, 3|Bile Duct Cancer|Biliary Tract Cancer|Prostate Cancer|Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome|Personality Disorder|Borderline Personality Disorder|Leukemia, Acute Myeloid|Schizophrenia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.