Variant (rsID / SNP)

rs2270191

rs2270191 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C6ORF15, C6orf15. Location: chromosome 6, position 31,080,320. The table records no clinical significance for this variant.

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Reference-table entries

C6ORF15Not classified

Variant type: missense_variant
Chromosome / position: 6:31080320
HGVS: NM_014070.3,c.13G>A,p.Val5Met
Allele change: Missense_V5M

Associated conditions / phenotypes

Inflammatory Bowel Disease|Ulcerative Colitis|Crohn's Disease

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.