Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs595986

IGSF9B

rs595986 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IGSF9B. Location: chromosome 11, position 133,814,191. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

IGSF9BNot classified
Variant type
synonymous_variant
Chromosome / position
11:133814191
HGVS
NM_001277285.4,c.333T>C,p.Tyr111Tyr
Allele change
Synonymous_Y111Y

Public references

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