List of variants in gene B9D1 reported as 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_015681.6(B9D1):c.472+28C>T	rs4924987	0.57381
NM_015681.6(B9D1):c.-70G>A	rs2296978	0.02165
NM_015681.6(B9D1):c.580T>C (p.Leu194=)	rs7212549	0.01478
NM_015681.6(B9D1):c.181C>T (p.Arg61Trp)	rs73980038	0.01073
NM_015681.6(B9D1):c.-110G>A	rs117169107	0.00495
NM_015681.6(B9D1):c.237C>G (p.Pro79=)	rs149051059	0.00295
NM_015681.6(B9D1):c.245-19C>A	rs774504181	0.00012
NM_015681.6(B9D1):c.516C>T (p.Asn172=)	rs149758860	0.00011
NM_015681.6(B9D1):c.597C>G (p.Pro199=)	rs753785719	0.00007
NM_001321218.2(B9D1):c.*61C>T	rs11652712

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