ClinVar Miner

List of variants reported as benign for Meckel syndrome, type 11 by Invitae

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
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HGVS dbSNP
NM_001077416.2(TMEM231):c.1050G>A (p.Val350=) rs149888762
NM_001077416.2(TMEM231):c.271C>G (p.Arg91Gly) rs375353411
NM_001077416.2(TMEM231):c.336G>C (p.Pro112=) rs78196225
NM_001077416.2(TMEM231):c.657G>A (p.Pro219=) rs201636741
NM_001077416.2(TMEM231):c.741+3A>G rs114290622
NM_001077416.2(TMEM231):c.741+8C>G rs144252983

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