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Variant (rsID / SNP)

rs690367

TP53BP1

rs690367 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TP53BP1. Location: chromosome 15, position 43,748,304. The table records no clinical significance for this variant.

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Reference-table entries

TP53BP1Not classified
Variant type
synonymous_variant
Chromosome / position
15:43748304
HGVS
NM_001141980.3,c.2502T>C,p.Asp834Asp
Allele change
Synonymous_D834D

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.