List of variants in gene DSP reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 24

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HGVS	dbSNP	gnomAD frequency
NM_004415.4(DSP):c.5213G>A (p.Arg1738Gln)	rs6929069	0.19612
NM_004415.4(DSP):c.4535A>G (p.Tyr1512Cys)	rs2076299	0.13777
NM_004415.4(DSP):c.913A>T (p.Ile305Phe)	rs17604693	0.02655
NM_004415.4(DSP):c.1903+7T>C	rs28763962	0.02605
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.2673T>C (p.Tyr891=)	rs146407262	0.00703
NM_004415.4(DSP):c.8300C>A (p.Thr2767Asn)	rs34884895	0.00701
NM_004415.4(DSP):c.*9T>A	rs11558732	0.00645
NM_004415.4(DSP):c.1481A>T (p.Tyr494Phe)	rs28763961	0.00618
NM_004415.4(DSP):c.1702-18C>T	rs148417566	0.00594
NM_004415.4(DSP):c.105G>A (p.Gly35=)	rs77445784	0.00587
NM_004415.4(DSP):c.8481C>T (p.Ser2827=)	rs151029175	0.00494
NM_004415.4(DSP):c.2630+18C>T	rs145963404	0.00475
NM_004415.4(DSP):c.6208G>A (p.Asp2070Asn)	rs41302885	0.00290
NM_004415.4(DSP):c.8455A>C (p.Met2819Leu)	rs138329459	0.00103
NM_004415.4(DSP):c.8605A>G (p.Ile2869Val)	rs28763971	0.00077
NM_004415.4(DSP):c.7548G>A (p.Arg2516=)	rs756527780	0.00006
NM_004415.4(DSP):c.12C>G (p.Asn4Lys)	rs368802003

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