Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs201738818

DOCK6

rs201738818 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DOCK6. Location: chromosome 19, position 11,319,669. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

DOCK6Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
19:11319669
Cytoband
19p13.2
HGVS
NM_020812.4(DOCK6):c.4862T>C (p.Val1621Ala)
Allele change
Missense_V1621A

Public references

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