Variant (rsID / SNP)

rs117522064

rs117522064 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDR81. Location: chromosome 17, position 1,639,350. Clinical significance in the table: Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

WDR81Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:1639350
Cytoband: 17p13.3
HGVS: NM_001163809.2(WDR81):c.5343C>T (p.Gly1781=)
Allele change: Synonymous_G730G

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.