Variant (rsID / SNP)

rs1132339

rs1132339 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNFAIP2. Location: chromosome 14, position 103,593,950. The table records no clinical significance for this variant.

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Reference-table entries

TNFAIP2Not classified

Variant type: missense_variant
Chromosome / position: 14:103593950
HGVS: NM_001371220.1,c.844C>G,p.Gln282Glu
Allele change: Missense_Q282E

Associated conditions / phenotypes

Autoimmune Disease|Multiple Sclerosis

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.