Variant (rsID / SNP)

rs3130100

rs3130100 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TAPBP. Location: chromosome 6, position 33,283,766. Clinical significance in the table: Benign.

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Reference-table entries

TAPBPBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:33283766
Cytoband: 6p21.32
HGVS: NM_005453.5(ZBTB22):c.928A>G (p.Thr310Ala)
Allele change: Missense_T310A

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.