List of variants in gene DSP reported as uncertain significance by Stanford Center for Inherited Cardiovascular Disease, Stanford University

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_004415.4(DSP):c.5498A>T (p.Glu1833Val)	rs78652302	0.00908
NM_004415.4(DSP):c.6208G>A (p.Asp2070Asn)	rs41302885	0.00290
NM_004415.4(DSP):c.4372C>G (p.Arg1458Gly)	rs28763965	0.00131
NM_004415.4(DSP):c.88G>A (p.Val30Met)	rs121912998	0.00094
NM_004415.4(DSP):c.6881C>G (p.Ala2294Gly)	rs147000526	0.00062
NM_004415.4(DSP):c.7916G>A (p.Arg2639Gln)	rs116888866	0.00026
NM_004415.4(DSP):c.5035C>T (p.His1679Tyr)	rs762561997	0.00021
NM_004415.4(DSP):c.269A>G (p.Gln90Arg)	rs188516326	0.00018
NM_004415.4(DSP):c.3706A>G (p.Arg1236Gly)	rs377098318	0.00016
NM_004415.4(DSP):c.943C>T (p.Arg315Cys)	rs200476515	0.00016
NM_004415.4(DSP):c.3862A>C (p.Lys1288Gln)	rs138907450	0.00014
NM_004415.4(DSP):c.889G>A (p.Asp297Asn)	rs201930322	0.00014
NM_004415.4(DSP):c.1140+6T>C	rs534740669	0.00010
NM_004415.4(DSP):c.4901G>A (p.Arg1634Gln)	rs144106775	0.00007
NM_004415.4(DSP):c.3338G>A (p.Arg1113Gln)	rs768455823	0.00006
NM_004415.4(DSP):c.1034A>G (p.Asp345Gly)	rs753855393	0.00005
NM_004415.4(DSP):c.6248G>A (p.Arg2083His)	rs574637009	0.00003
NM_004415.4(DSP):c.7915C>T (p.Arg2639Trp)	rs771553674	0.00003
NM_004415.4(DSP):c.3877A>G (p.Ile1293Val)	rs376555665	0.00002
NM_004415.4(DSP):c.6269A>G (p.Glu2090Gly)	rs755069593	0.00002
NM_004415.4(DSP):c.1562A>C (p.Asp521Ala)	rs748790273	0.00001
NM_004415.4(DSP):c.2071C>T (p.Leu691Phe)	rs1363445022	0.00001
NM_004415.4(DSP):c.2933T>A (p.Ile978Lys)	rs1060500615	0.00001
NM_004415.4(DSP):c.3200C>T (p.Ala1067Val)	rs1317030435	0.00001
NM_004415.4(DSP):c.6902T>C (p.Ile2301Thr)	rs772381363	0.00001
NM_004415.4(DSP):c.7885G>A (p.Glu2629Lys)	rs756976948	0.00001
NM_004415.4(DSP):c.1090A>G (p.Ile364Val)	rs886038909
NM_004415.4(DSP):c.5353G>A (p.Glu1785Lys)	rs528041468
NM_004415.4(DSP):c.8529_8540del (p.2827_2830SGSR[4])	rs794728151
NM_004415.4(DSP):c.935_937del (p.Phe312del)	rs794728138

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