List of variants in gene DSP reported as benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 49

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HGVS	dbSNP	gnomAD frequency
NM_004415.4(DSP):c.1dup (p.Met1fs)	rs17133512	0.17362
NM_004415.4(DSP):c.423-16_423-15insC	rs113028223	0.03015
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.5498A>T (p.Glu1833Val)	rs78652302	0.00908
NM_004415.4(DSP):c.2673T>C (p.Tyr891=)	rs146407262	0.00703
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.2630+18C>T	rs145963404	0.00475
NM_004415.4(DSP):c.4383G>A (p.Glu1461=)	rs140029036	0.00197
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.1920C>T (p.Ile640=)	rs74806300	0.00156
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.522T>C (p.Cys174=)	rs144781697	0.00124
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.7734C>T (p.Ser2578=)	rs28763970	0.00087
NM_004415.4(DSP):c.741G>A (p.Ala247=)	rs2806234	0.00083
NM_004415.4(DSP):c.8605A>G (p.Ile2869Val)	rs28763971	0.00077
NM_004415.4(DSP):c.4065T>C (p.Tyr1355=)	rs148478829	0.00073
NM_004415.4(DSP):c.1778A>G (p.Asn593Ser)	rs34239595	0.00055
NM_004415.4(DSP):c.8019C>T (p.Asp2673=)	rs144275591	0.00047
NM_004415.4(DSP):c.8301C>G (p.Thr2767=)	rs145362059	0.00046
NM_004415.4(DSP):c.3123C>T (p.Leu1041=)	rs149929637	0.00042
NM_004415.4(DSP):c.2723G>A (p.Arg908His)	rs142494121	0.00041
NM_004415.4(DSP):c.4500G>T (p.Leu1500=)	rs372881903	0.00039
NM_004415.4(DSP):c.3923G>A (p.Arg1308Gln)	rs184154918	0.00037
NM_004415.4(DSP):c.7916G>A (p.Arg2639Gln)	rs116888866	0.00026
NM_004415.4(DSP):c.1344G>A (p.Leu448=)	rs138226280	0.00019
NM_004415.4(DSP):c.6351T>C (p.Asp2117=)	rs148743859	0.00019
NM_004415.4(DSP):c.8415C>T (p.Ala2805=)	rs377148997	0.00019
NM_004415.4(DSP):c.1140+6T>C	rs534740669	0.00010
NM_004415.4(DSP):c.2437-20T>G	rs778134276	0.00006
NM_004415.4(DSP):c.4320G>A (p.Val1440=)	rs571103583	0.00006
NM_004415.4(DSP):c.7548G>A (p.Arg2516=)	rs756527780	0.00006
NM_004415.4(DSP):c.8268A>C (p.Ile2756=)	rs397516963	0.00006
NM_004415.4(DSP):c.3507C>T (p.Tyr1169=)	rs148894066	0.00005
NM_004415.4(DSP):c.264C>T (p.Ile88=)	rs727502997	0.00004
NM_004415.4(DSP):c.3303C>T (p.Tyr1101=)	rs372440854	0.00002
NM_004415.4(DSP):c.6655G>A (p.Val2219Ile)	rs397516953	0.00002
NM_004415.4(DSP):c.8191T>C (p.Tyr2731His)	rs201397978	0.00001
NM_004415.4(DSP):c.1266+6G>T	rs73375345
NM_004415.4(DSP):c.2436+16A>G	rs199555263
NM_004415.4(DSP):c.8496ATCTCGCTCCGG[1] (p.2827SGSR[4])	rs397516971

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