List of variants in gene SPRED1 reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 21

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HGVS	dbSNP	gnomAD frequency
NM_152594.3(SPRED1):c.291G>A (p.Lys97=)	rs7182445	0.82029
NM_152594.3(SPRED1):c.424-8C>A	rs7180446	0.82015
NM_152594.3(SPRED1):c.1044T>C (p.Val348=)	rs3751526	0.81965
NM_152594.3(SPRED1):c.*4662T>A	rs10852019	0.77666
NM_152594.3(SPRED1):c.*5110C>T	rs8026118	0.76725
NM_152594.3(SPRED1):c.*3830G>A	rs8039150	0.22628
NM_152594.3(SPRED1):c.*4932A>G	rs16966843	0.20289
NM_152594.3(SPRED1):c.*2831G>A	rs35490364	0.19653
NM_152594.3(SPRED1):c.*3521A>G	rs11634702	0.11111
NM_152594.3(SPRED1):c.*1724A>C	rs1554527	0.08749
NM_152594.3(SPRED1):c.*3996G>A	rs72725364	0.08710
NM_152594.3(SPRED1):c.*248T>C	rs16966842	0.04503
NM_152594.3(SPRED1):c.*256C>T	rs145373657	0.01162
NM_152594.3(SPRED1):c.*3698T>G	rs76527876	0.00908
NM_152594.3(SPRED1):c.-93C>T	rs192699510	0.00724
NM_152594.3(SPRED1):c.583-7A>G	rs115970207	0.00630
NM_152594.3(SPRED1):c.*427A>T	rs185290497	0.00592
NM_152594.3(SPRED1):c.*2742G>T	rs149336440	0.00260
NM_152594.3(SPRED1):c.*5398G>T	rs115003524	0.00257
NM_152594.3(SPRED1):c.926T>C (p.Val309Ala)	rs114636635	0.00204
NM_152594.3(SPRED1):c.*3946G>A	rs8039337

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