Variant (rsID / SNP)
rs9379084
rs9379084 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RREB1. Location: chromosome 6, position 7,231,843. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- missense_variant
- Chromosome / position
- 6:7231843
- HGVS
- NM_001003699.4,c.3511G>A,p.Asp1171Asn
- Allele change
- Missense_D1171N
Associated conditions / phenotypes
Kidney Disease|Body Mass Index Quantitative Trait Locus 11|Body Mass Index Quantitative Trait Locus 18|Body Mass Index Quantitative Trait Locus 19|Body Mass Index Quantitative Trait Locus 10|Body Mass Index Quantitative Trait Locus 7|Body Mass Index Quantitative Trait Locus 4|Body Mass Index Quantitative Trait Locus 12|Body Mass Index Quantitative Trait Locus 14|Body Mass Index Quantitative Trait Locus 9|Body Mass Index Quantitative Trait Locus 8|Gestational Diabetes|Diabetes Mellitus
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.