List of variants reported as likely benign for Prune belly syndrome by Fulgent Genetics, Fulgent Genetics

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001375978.1(CHRM3):c.328C>T (p.Leu110=)	rs111407169	0.00033
NM_001375978.1(CHRM3):c.1152C>T (p.Pro384=)	rs139780487	0.00028
NM_001375978.1(CHRM3):c.681T>C (p.Ser227=)	rs199549014	0.00011
NM_001375978.1(CHRM3):c.1354G>T (p.Ala452Ser)
NM_001375978.1(CHRM3):c.1709A>C (p.Lys570Thr)

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