Variant (rsID / SNP)

rs33980500

rs33980500 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRAF3IP2. Location: chromosome 6, position 111,913,262. Clinical significance in the table: Benign.

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Reference-table entries

TRAF3IP2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:111913262
Cytoband: 6q21
HGVS: NM_147686.4(TRAF3IP2):c.28G>A (p.Asp10Asn)
Allele change: Silent

Associated conditions / phenotypes

Psoriasis 13, susceptibility to|Candidiasis, familial, 8

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.