List of variants in gene B9D2 reported as likely benign for Meckel syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_030578.4(B9D2):c.88+6C>T	rs112498529	0.00205
NM_030578.4(B9D2):c.336G>A (p.Thr112=)	rs139072904	0.00027
NM_030578.4(B9D2):c.151A>C (p.Ile51Leu)	rs368393895	0.00024
NM_030578.4(B9D2):c.224G>A (p.Arg75Gln)	rs148087680	0.00016
NM_030578.4(B9D2):c.309G>A (p.Pro103=)	rs201735642	0.00004
NM_030578.4(B9D2):c.495C>T (p.Leu165=)	rs542445852	0.00004
NM_030578.4(B9D2):c.89-15C>T	rs371483684	0.00004
NM_030578.4(B9D2):c.132G>A (p.Thr44=)
NM_030578.4(B9D2):c.186C>T (p.Asp62=)
NM_030578.4(B9D2):c.346C>T (p.Leu116=)	rs1555755825
NM_030578.4(B9D2):c.432C>T (p.Ala144=)
NM_030578.4(B9D2):c.516C>T (p.Gly172=)
NM_030578.4(B9D2):c.88+17G>C

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