Variant (rsID / SNP)

rs16844422

rs16844422 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DOK7. Location: chromosome 4, position 3,487,322. Clinical significance in the table: Benign.

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Reference-table entries

DOK7Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:3487322
Cytoband: 4p16.3
HGVS: NM_173660.5(DOK7):c.589G>A (p.Asp197Asn)
Allele change: Missense_D53N

Associated conditions / phenotypes

Fetal akinesia deformation sequence 1|Congenital myasthenic syndrome 10

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.