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Variant (rsID / SNP)

rs11155787

ZBTB2

rs11155787 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZBTB2. Location: chromosome 6, position 151,686,905. The table records no clinical significance for this variant.

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Reference-table entries

ZBTB2Not classified
Variant type
synonymous_variant
Chromosome / position
6:151686905
HGVS
NM_020861.3,c.1296G>A,p.Glu432Glu
Allele change
Synonymous_E432E

Public references

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