Variant (rsID / SNP)

rs2241880

rs2241880 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATG16L1. Location: chromosome 2, position 234,183,368. Clinical significance in the table: Benign.

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Reference-table entries

ATG16L1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:234183368
Cytoband: 2q37.1
HGVS: NM_030803.7(ATG16L1):c.898A>G (p.Thr300Ala)
Allele change: Missense_T281A

Associated conditions / phenotypes

Inflammatory bowel disease 10, susceptibility to

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.