Variant (rsID / SNP)

rs2228397

rs2228397 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TAP2. Location: chromosome 6, position 32,800,224. Clinical significance in the table: Benign.

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Reference-table entries

TAP2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:32800224
Cytoband: 6p21.32
HGVS: NM_001290043.2(TAP2):c.1158G>T (p.Gly386=)
Allele change: Synonymous_G386G

Associated conditions / phenotypes

MHC class I deficiency

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.