List of variants in gene ADAMTS13 reported as benign by PreventionGenetics, part of Exact Sciences

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_139027.6(ADAMTS13):c.1342C>G (p.Gln448Glu)	rs2301612	0.31482
NM_139027.6(ADAMTS13):c.4053C>A (p.Thr1351=)	rs1055432	0.26164
NM_139027.6(ADAMTS13):c.2699C>T (p.Ala900Val)	rs685523	0.10882
NM_139027.6(ADAMTS13):c.19C>T (p.Arg7Trp)	rs34024143	0.09518
NM_139027.6(ADAMTS13):c.987+11C>T	rs28729234	0.09160
NM_139027.6(ADAMTS13):c.1852C>G (p.Pro618Ala)	rs28647808	0.05902
NM_139027.6(ADAMTS13):c.686+4T>G	rs36219245	0.05749
NM_139027.6(ADAMTS13):c.582C>T (p.Gly194=)	rs34054981	0.05724
NM_139027.6(ADAMTS13):c.354G>A (p.Pro118=)	rs28571612	0.05636
NM_139027.6(ADAMTS13):c.173-48G>A	rs35194094	0.05607
NM_139027.6(ADAMTS13):c.173-18C>T	rs35410697	0.04598
NM_139027.6(ADAMTS13):c.3108G>A (p.Ser1036=)	rs34934621	0.03291
NM_139027.6(ADAMTS13):c.3045-41G>A	rs34100568	0.03287
NM_139027.6(ADAMTS13):c.3045-48T>C	rs36023469	0.03287
NM_139027.6(ADAMTS13):c.2910C>T (p.Val970=)	rs28641026	0.03155
NM_139027.6(ADAMTS13):c.3097G>A (p.Ala1033Thr)	rs28503257	0.03107
NM_139027.6(ADAMTS13):c.1874G>A (p.Arg625His)	rs36090624	0.02177
NM_139027.6(ADAMTS13):c.1368G>T (p.Gln456His)	rs36220239	0.01611
NM_139027.6(ADAMTS13):c.936C>T (p.Arg312=)	rs36219562	0.01608
NM_139027.6(ADAMTS13):c.2508T>C (p.Asp836=)	rs36221472	0.01405
NM_139027.6(ADAMTS13):c.2218G>A (p.Glu740Lys)	rs36221451	0.01123
NM_139027.6(ADAMTS13):c.1797C>T (p.Ile599=)	rs36221216	0.01122
NM_139027.6(ADAMTS13):c.540-33G>A	rs36218903	0.01059
NM_139027.6(ADAMTS13):c.3250-19T>C	rs36222582	0.00936
NM_139027.6(ADAMTS13):c.3678G>A (p.Val1226=)	rs36222899	0.00845
NM_139027.6(ADAMTS13):c.357C>T (p.Ser119=)	rs147563206	0.00731
NM_139027.6(ADAMTS13):c.3287G>A (p.Arg1096His)	rs61751476	0.00571
NM_139027.6(ADAMTS13):c.1705+7G>A	rs78739717	0.00233
NM_139027.6(ADAMTS13):c.3159G>A (p.Ala1053=)	rs200349242	0.00004

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