List of variants reported as likely benign for Bardet-Biedl syndrome 4 by Fulgent Genetics, Fulgent Genetics

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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_033028.5(BBS4):c.712-17C>G	rs150754122	0.01051
NM_033028.5(BBS4):c.460-20T>C	rs200203402	0.00048
NM_033028.5(BBS4):c.157-19A>G	rs373166573	0.00046
NM_033028.5(BBS4):c.24+8C>T	rs200055760	0.00040
NM_033028.5(BBS4):c.24+18C>G	rs368789560	0.00034
NM_033028.5(BBS4):c.1107-11G>C	rs373344695	0.00020
NM_033028.5(BBS4):c.643-6T>C	rs753675755	0.00006
NM_033028.5(BBS4):c.1170C>T (p.Asn390=)	rs376378002	0.00005
NM_033028.5(BBS4):c.76+18dup	rs745516764	0.00005
NM_033028.5(BBS4):c.1311C>G (p.Thr437=)	rs945847885	0.00004
NM_033028.5(BBS4):c.501C>T (p.His167=)	rs745789574	0.00004
NM_033028.5(BBS4):c.712-14T>A	rs375598833	0.00004
NM_033028.5(BBS4):c.928T>C (p.Leu310=)	rs375714932	0.00003
NM_033028.5(BBS4):c.408G>A (p.Glu136=)	rs201881253	0.00001
NM_033028.5(BBS4):c.1223_1225dup (p.Asn408dup)	rs752690768
NM_033028.5(BBS4):c.712-15G>C	rs2065814889
NM_033028.5(BBS4):c.943T>C (p.Leu315=)	rs1433729329

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