ClinVar Miner

List of variants in gene TTC39A studied for muscle tissue disorder

Included ClinVar conditions (1088):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_001297663.2(TTC39A):c.1322C>T (p.Thr441Met) rs756251338 0.00001
NM_001297663.2(TTC39A):c.1490C>G (p.Ala497Gly) rs1553171591

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