Variant (rsID / SNP)

rs2498946

rs2498946 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DOCK1. Location: chromosome 10, position 129,070,313. The table records no clinical significance for this variant.

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Reference-table entries

DOCK1Not classified

Variant type: missense_variant
Chromosome / position: 10:129070313
HGVS: NM_001377561.1,c.3083G>A,p.Gly1028Glu
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.