List of variants in gene SPRED1 reported as likely benign for not provided

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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: 31

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HGVS	dbSNP	gnomAD frequency
NM_152594.3(SPRED1):c.*256C>T	rs145373657	0.01162
NM_152594.3(SPRED1):c.684+133A>G	rs76305448	0.01099
NM_152594.3(SPRED1):c.-332G>A	rs147075186	0.00717
NM_152594.3(SPRED1):c.32+162G>A	rs142573328	0.00345
NM_152594.3(SPRED1):c.377-201A>G	rs139396722	0.00283
NM_152594.3(SPRED1):c.926T>C (p.Val309Ala)	rs114636635	0.00204
NM_152594.3(SPRED1):c.675C>T (p.Ser225=)	rs144764225	0.00092
NM_152594.3(SPRED1):c.207+15A>G	rs377288061	0.00073
NM_152594.3(SPRED1):c.*4471C>A	rs574232846	0.00071
NM_152594.3(SPRED1):c.939G>A (p.Thr313=)	rs140644874	0.00070
NM_152594.3(SPRED1):c.*3192G>A	rs566065329	0.00064
NM_152594.3(SPRED1):c.377-10A>G	rs376134678	0.00026
NM_152594.3(SPRED1):c.*4304G>A	rs537477031	0.00017
NM_152594.3(SPRED1):c.963G>A (p.Lys321=)	rs369711772	0.00011
NM_152594.3(SPRED1):c.177T>C (p.Phe59=)	rs397517871	0.00010
NM_152594.3(SPRED1):c.26A>T (p.Asp9Val)	rs200157475	0.00010
NM_152594.3(SPRED1):c.1192G>A (p.Asp398Asn)	rs771480941	0.00009
NM_152594.3(SPRED1):c.1176G>A (p.Ser392=)	rs755223172	0.00005
NM_152594.3(SPRED1):c.685-8T>C	rs760690837	0.00005
NM_152594.3(SPRED1):c.594T>C (p.Gly198=)	rs756643495	0.00004
NM_152594.3(SPRED1):c.684+50A>T	rs200338097	0.00003
NM_152594.3(SPRED1):c.1005C>T (p.Cys335=)	rs768937237	0.00002
NM_152594.3(SPRED1):c.879G>A (p.Leu293=)	rs535687467	0.00002
NM_152594.3(SPRED1):c.384C>T (p.Pro128=)	rs761058615	0.00001
NC_000015.10:g.38252630G>T	rs569895675
NM_152594.3(SPRED1):c.*3647T>G	rs186366365
NM_152594.3(SPRED1):c.1110C>T (p.Leu370=)
NM_152594.3(SPRED1):c.1225_1226delinsTT (p.Ala409Phe)
NM_152594.3(SPRED1):c.183T>G (p.Arg61=)
NM_152594.3(SPRED1):c.636A>C (p.Val212=)	rs1057523137
NM_152594.3(SPRED1):c.933T>C (p.Phe311=)	rs1057522873

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