Variant (rsID / SNP)
rs12103
rs12103 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to INTS11. Location: chromosome 1, position 1,247,494. The table records no clinical significance for this variant.
Reference-table entries
INTS11Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 1:1247494
- HGVS
- NM_001256456.2,c.1659A>G,p.Pro553Pro
- Allele change
- Synonymous_P547P
Associated conditions / phenotypes
Inflammatory Bowel Disease|Crohn's Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.