Variant (rsID / SNP)
rs7498665
rs7498665 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SH2B1. Location: chromosome 16, position 28,883,241. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- missense_variant
- Chromosome / position
- 16:28883241
- HGVS
- NM_001145795.2,c.1450A>G,p.Thr484Ala
- Allele change
- Missense_T484A
Associated conditions / phenotypes
Lipid Metabolism Disorder|Body Mass Index Quantitative Trait Locus 14|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 9|Body Mass Index Quantitative Trait Locus 8|Leptin Deficiency or Dysfunction|Body Mass Index Quantitative Trait Locus 1|Schizophrenia|Type 2 Diabetes Mellitus
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.