List of variants in gene BSND reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_057176.3(BSND):c.924G>A (p.Pro308=)	rs33938617	0.18512
NM_057176.3(BSND):c.177+11G>A	rs78904893	0.06761
NM_057176.3(BSND):c.127G>A (p.Val43Ile)	rs34561376	0.04587
NM_057176.3(BSND):c.272+20G>A	rs79445756	0.04480
NM_057176.3(BSND):c.459C>T (p.Asp153=)	rs138974602	0.00328
NM_057176.3(BSND):c.63C>T (p.Leu21=)	rs141611486	0.00079
NM_057176.3(BSND):c.141G>C (p.Gly47=)	rs76222905	0.00053
NM_057176.3(BSND):c.69G>A (p.Thr23=)	rs368632305	0.00032
NM_057176.3(BSND):c.702G>A (p.Pro234=)	rs148085906	0.00019
NM_057176.3(BSND):c.139G>A (p.Gly47Arg)	rs74315289	0.00016
NM_057176.3(BSND):c.16A>G (p.Thr6Ala)	rs201342416	0.00013
NM_057176.3(BSND):c.570C>T (p.Gly190=)	rs368273749	0.00002
NM_057176.3(BSND):c.526C>T (p.Arg176Cys)

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