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Variant (rsID / SNP)

rs222837

DVL2

rs222837 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DVL2. Location: chromosome 17, position 7,132,556. The table records no clinical significance for this variant.

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Reference-table entries

DVL2Not classified
Variant type
synonymous_variant
Chromosome / position
17:7132556
HGVS
NM_004422.3,c.855G>A,p.Gln285Gln
Allele change
Synonymous_Q285Q

Public references

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