List of variants in gene DSP reported as likely 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: 22

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HGVS	dbSNP	gnomAD frequency
NM_004415.4(DSP):c.4455G>T (p.Arg1485Ser)	rs113902911	0.00572
NM_004415.4(DSP):c.1206G>A (p.Lys402=)	rs150422458	0.00185
NM_004415.4(DSP):c.4489C>T (p.Arg1497Trp)	rs148041814	0.00178
NM_004415.4(DSP):c.6678T>A (p.Gly2226=)	rs149070106	0.00139
NM_004415.4(DSP):c.3696C>A (p.Ser1232=)	rs141120358	0.00132
NM_004415.4(DSP):c.4372C>G (p.Arg1458Gly)	rs28763965	0.00131
NM_004415.4(DSP):c.2346C>T (p.Asp782=)	rs139071827	0.00126
NM_004415.4(DSP):c.7734C>T (p.Ser2578=)	rs28763970	0.00087
NM_004415.4(DSP):c.741G>A (p.Ala247=)	rs2806234	0.00083
NM_004415.4(DSP):c.6881C>G (p.Ala2294Gly)	rs147000526	0.00062
NM_004415.4(DSP):c.2723G>A (p.Arg908His)	rs142494121	0.00041
NM_004415.4(DSP):c.6319G>C (p.Val2107Leu)	rs144263721	0.00036
NM_004415.4(DSP):c.6753G>A (p.Lys2251=)	rs750294829	0.00011
NM_004415.4(DSP):c.687C>T (p.Gly229=)	rs112877191	0.00011
NM_004415.4(DSP):c.816G>A (p.Leu272=)	rs376184294	0.00011
NM_004415.4(DSP):c.3981C>T (p.Ile1327=)	rs397516934	0.00009
NM_004415.4(DSP):c.3231G>A (p.Ala1077=)	rs368214030	0.00003
NM_004415.4(DSP):c.1065G>A (p.Gln355=)	rs750289780	0.00001
NM_004415.4(DSP):c.2418T>C (p.Ala806=)	rs1759183681
NM_004415.4(DSP):c.2631-10T>A	rs369840498
NM_004415.4(DSP):c.3084+8A>T
NM_004415.4(DSP):c.8111AGA[2] (p.Lys2706del)	rs397516962

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