Variant (rsID / SNP)
rs2077647
rs2077647 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ESR1. Location: chromosome 6, position 152,129,077. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- synonymous_variant
- Chromosome / position
- 6:152129077
- HGVS
- NM_001291230.2,c.30T>C,p.Ser10Ser
- Allele change
- Synonymous_S10S
Associated conditions / phenotypes
Hepatitis B|Hypospadias|Mammographic Density|Breast Cancer|Dental Fluorosis|Prostate Cancer|Down Syndrome|Osteoporosis|Infantile Liver Failure Syndrome 1|Leukemia, Acute Myeloid|Cryptorchidism, Unilateral or Bilateral|Bone Mineral Density Quantitative Trait Locus 15|Bone Mineral Density Quantitative Trait Locus 8|Liver Disease|Postpartum Depression|Osteoarthritis|Mood Disorder|Liver Cirrhosis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.