List of variants in gene DSP reported as likely benign by Biesecker Lab/Clinical Genomics Section, National Institutes of Health

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_004415.4(DSP):c.6208G>A (p.Asp2070Asn)	rs41302885	0.00290
NM_004415.4(DSP):c.4588G>T (p.Val1530Phe)	rs141227126	0.00197
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.782C>T (p.Ala261Val)	rs139509870	0.00067
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.688G>A (p.Asp230Asn)	rs147315869	0.00038
NM_004415.4(DSP):c.5178C>A (p.Asn1726Lys)	rs147415451	0.00033
NM_004415.4(DSP):c.3297G>C (p.Lys1099Asn)	rs370550974	0.00025
NM_004415.4(DSP):c.4750G>A (p.Ala1584Thr)	rs191778417	0.00009
NM_004415.4(DSP):c.4741A>G (p.Lys1581Glu)	rs186842903	0.00003
NM_004415.4(DSP):c.8191T>C (p.Tyr2731His)	rs201397978	0.00001
NM_004415.4(DSP):c.4034A>C (p.Glu1345Ala)	rs201964660

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