List of variants in gene DSP reported as likely benign for Arrhythmogenic right ventricular dysplasia 8

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: 41

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HGVS	dbSNP	gnomAD frequency
NM_004415.4(DSP):c.913A>T (p.Ile305Phe)	rs17604693	0.02655
NM_004415.4(DSP):c.273+10C>T	rs56148603	0.02451
NM_004415.4(DSP):c.4773G>A (p.Arg1591=)	rs28763968	0.01341
NM_004415.4(DSP):c.2815G>A (p.Gly939Ser)	rs80325569	0.01244
NM_004415.4(DSP):c.3963G>A (p.Gln1321=)	rs61731476	0.01161
NM_004415.4(DSP):c.3510G>A (p.Glu1170=)	rs28763964	0.01023
NM_004415.4(DSP):c.6390T>C (p.Ala2130=)	rs28763969	0.00940
NM_004415.4(DSP):c.4609C>T (p.Arg1537Cys)	rs28763967	0.00925
NM_004415.4(DSP):c.5498A>T (p.Glu1833Val)	rs78652302	0.00908
NM_004415.4(DSP):c.*9T>A	rs11558732	0.00645
NM_004415.4(DSP):c.105G>A (p.Gly35=)	rs77445784	0.00587
NM_004415.4(DSP):c.4455G>T (p.Arg1485Ser)	rs113902911	0.00572
NM_004415.4(DSP):c.8481C>T (p.Ser2827=)	rs151029175	0.00494
NM_004415.4(DSP):c.6208G>A (p.Asp2070Asn)	rs41302885	0.00290
NM_004415.4(DSP):c.4141A>T (p.Thr1381Ser)	rs77758574	0.00270
NM_004415.4(DSP):c.7995G>A (p.Thr2665=)	rs35379048	0.00265
NM_004415.4(DSP):c.4383G>A (p.Glu1461=)	rs140029036	0.00197
NM_004415.4(DSP):c.4588G>T (p.Val1530Phe)	rs141227126	0.00197
NM_004415.4(DSP):c.1488G>A (p.Thr496=)	rs35820473	0.00195
NM_004415.4(DSP):c.2773C>T (p.Arg925Trp)	rs145933612	0.00143
NM_004415.4(DSP):c.4372C>G (p.Arg1458Gly)	rs28763965	0.00131
NM_004415.4(DSP):c.8455A>C (p.Met2819Leu)	rs138329459	0.00103
NM_004415.4(DSP):c.88G>A (p.Val30Met)	rs121912998	0.00094
NM_004415.4(DSP):c.5218G>A (p.Glu1740Lys)	rs142885240	0.00091
NM_004415.4(DSP):c.8605A>G (p.Ile2869Val)	rs28763971	0.00077
NM_004415.4(DSP):c.6881C>G (p.Ala2294Gly)	rs147000526	0.00062
NM_004415.4(DSP):c.1778A>G (p.Asn593Ser)	rs34239595	0.00055
NM_004415.4(DSP):c.2723G>A (p.Arg908His)	rs142494121	0.00041
NM_004415.4(DSP):c.5167G>C (p.Glu1723Gln)	rs142803672	0.00041
NM_004415.4(DSP):c.5178C>A (p.Asn1726Lys)	rs147415451	0.00033
NM_004415.4(DSP):c.*47T>C	rs376397291	0.00026
NM_004415.4(DSP):c.1696G>A (p.Ala566Thr)	rs148147581	0.00026
NM_004415.4(DSP):c.7916G>A (p.Arg2639Gln)	rs116888866	0.00026
NM_004415.4(DSP):c.8467C>G (p.Pro2823Ala)	rs142717240	0.00020
NM_004415.4(DSP):c.269A>G (p.Gln90Arg)	rs188516326	0.00018
NM_004415.4(DSP):c.889G>A (p.Asp297Asn)	rs201930322	0.00014
NM_004415.4(DSP):c.7278T>C (p.Tyr2426=)	rs78843072	0.00010
NM_004415.4(DSP):c.5513G>A (p.Arg1838His)	rs377715841	0.00009
NM_004415.4(DSP):c.4741A>G (p.Lys1581Glu)	rs186842903	0.00003
NM_004415.4(DSP):c.5593A>T (p.Asn1865Tyr)	rs562015789	0.00001
NM_004415.4(DSP):c.8191T>C (p.Tyr2731His)	rs201397978	0.00001

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