ClinVar Miner

List of variants reported as likely benign for fetal lower urinary tract obstruction

Included ClinVar conditions (2):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001375978.1(CHRM3):c.328C>T (p.Leu110=)	rs111407169	0.00037
NM_001375978.1(CHRM3):c.1152C>T (p.Pro384=)	rs139780487	0.00026
NM_001375978.1(CHRM3):c.681T>C (p.Ser227=)	rs199549014	0.00012

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