ClinVar Miner

List of variants in gene TMEM237 reported as uncertain significance for Joubert syndrome 1

Included ClinVar conditions (11):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_001044385.3(TMEM237):c.*258del rs558670305 0.00075
NM_001044385.3(TMEM237):c.*714_*715del rs373844800 0.00014
NM_001044385.3(TMEM237):c.*3513del rs143218667
NM_001044385.3(TMEM237):c.*470_*473del rs886055445

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