Variant (rsID / SNP)
rs35494829
rs35494829 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SUCLG2. Location: chromosome 3, position 67,426,281. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- missense_variant&splice_region_variant
- Chromosome / position
- 3:67426281
- HGVS
- NM_003848.4,c.1186A>G,p.Thr396Ala
- Allele change
- Silent
Associated conditions / phenotypes
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|Colorectal Cancer|Body Mass Index Quantitative Trait Locus 14|Body Mass Index Quantitative Trait Locus 9|Body Mass Index Quantitative Trait Locus 8
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.