Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs117316062

KATNIP

rs117316062 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KATNIP. Location: chromosome 16, position 27,784,497. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

KATNIPNot classified
Variant type
missense_variant
Chromosome / position
16:27784497
HGVS
NM_015202.5,c.4276G>A,p.Glu1426Lys
Allele change
Missense_E1426K

Public references

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