Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs4236176

WDR27

rs4236176 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDR27. Location: chromosome 6, position 170,070,723. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

WDR27Not classified
Variant type
missense_variant
Chromosome / position
6:170070723
HGVS
NM_182552.5,c.398T>C,p.Leu133Pro
Allele change
Missense_L133P

Associated conditions / phenotypes

Missense_L133P

Public references

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