ClinVar Miner

List of variants in gene B9D1, LOC130060455 studied for Meckel syndrome, type 9

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_015681.6(B9D1):c.63+23G>A	rs10445411	0.56182
NM_015681.6(B9D1):c.-42C>T	rs750522077	0.00002
NM_015681.6(B9D1):c.-21C>T	rs1911267997
NM_015681.6(B9D1):c.9C>G (p.Thr3=)	rs749611797

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