Variant (rsID / SNP)

rs3781411

rs3781411 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CTBP2. Location: chromosome 10, position 126,715,436. The table records no clinical significance for this variant.

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Reference-table entries

CTBP2Not classified

Variant type: missense_variant
Chromosome / position: 10:126715436
HGVS: NM_022802.3,c.893G>A,p.Arg298Gln
Allele change: Silent

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.