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Variant (rsID / SNP)

rs2243191

IL19

rs2243191 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL19. Location: chromosome 1, position 207,015,957. The table records no clinical significance for this variant.

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Reference-table entries

IL19Not classified
Variant type
missense_variant
Chromosome / position
1:207015957
HGVS
NM_001369605.1,c.524T>C,p.Phe175Ser
Allele change
Missense_F213S

Associated conditions / phenotypes

Colitis|Hepatitis B|Hepatitis|Ulcerative Colitis

Public references

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