List of variants reported as benign for Meckel syndrome by Fulgent Genetics, Fulgent Genetics

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000660.7(TGFB1):c.29C>T (p.Pro10Leu)	rs1800470	0.60129
NM_015272.5(RPGRIP1L):c.3395A>G (p.Gln1132Arg)	rs561414163	0.00004

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