Variant (rsID / SNP)

rs16870908

rs16870908 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TAP2. Location: chromosome 6, position 32,790,089. 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: 6:32790089
Cytoband: 6p21.32
HGVS: NM_018833.3(TAP2):c.1939C>T (p.Leu647Phe)
Allele change: Missense_L647F

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.