Variant (rsID / SNP)

rs147554257

rs147554257 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DOCK6. Location: chromosome 19, position 11,325,084. Clinical significance in the table: Benign/Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

DOCK6Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 19:11325084
Cytoband: 19p13.2
HGVS: NM_020812.4(DOCK6):c.4205C>T (p.Thr1402Met)
Allele change: Missense_T1402M

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.