Variant (rsID / SNP)

rs3763048

rs3763048 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DOCK2. Location: chromosome 5, position 169,461,547. The table records no clinical significance for this variant.

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Reference-table entries

DOCK2Not classified

Variant type: synonymous_variant
Chromosome / position: 5:169461547
HGVS: NM_004946.3,c.3612C>T,p.Thr1204Thr
Allele change: Synonymous_T1204T

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.