Variant (rsID / SNP)

rs76296365

rs76296365 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM237. Location: chromosome 2, position 202,503,779. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

TMEM237Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 2:202503779
Cytoband: 2q33.1
HGVS: NM_001044385.3(TMEM237):c.80-11T>C
Allele change: Silent

Associated conditions / phenotypes

Joubert syndrome 14

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.