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Variant (rsID / SNP)

rs4708711

DACT2

rs4708711 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DACT2. Location: chromosome 6, position 168,695,345. The table records no clinical significance for this variant.

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Reference-table entries

DACT2Not classified
Variant type
missense_variant
Chromosome / position
6:168695345
HGVS
NM_001286351.2,c.698C>T,p.Pro233Leu
Allele change
Missense_P233L

Public references

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