Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs59493015

TMEM216

rs59493015 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM216. Location: chromosome 11, position 61,160,080. Clinical significance in the table: Benign/Likely benign.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

TMEM216Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
11:61160080
Cytoband
11q12.2
HGVS
NM_001173990.3(TMEM216):c.-24C>G
Allele change
Silent

Associated conditions / phenotypes

Meckel syndrome, type 2|Joubert syndrome 2

Public references

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