List of variants in gene CLASP1, RNU4ATAC studied for Roifman syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001395891.1(CLASP1):c.196-567G>A	rs559979281	0.00038
NM_001395891.1(CLASP1):c.196-605C>T	rs188343279	0.00038
NM_001395891.1(CLASP1):c.196-562G>A	rs370715569	0.00025
NM_001395891.1(CLASP1):c.196-591C>T	rs756026847	0.00013
NM_001395891.1(CLASP1):c.196-572C>T	rs991806266	0.00008
NM_001395891.1(CLASP1):c.196-602C>T	rs863225422	0.00005
NM_001395891.1(CLASP1):c.196-678C>T	rs544312701	0.00004
NM_001395891.1(CLASP1):c.196-672A>G	rs863225423	0.00002
NM_001395891.1(CLASP1):c.196-571C>T	rs765906028	0.00001
NM_001395891.1(CLASP1):c.196-562G>C
NM_001395891.1(CLASP1):c.196-570C>T	rs750325275
NM_001395891.1(CLASP1):c.196-600C>T	rs1032667950
NM_001395891.1(CLASP1):c.196-604C>T	rs181195449
NM_001395891.1(CLASP1):c.196-670T>A	rs982261295
NM_001395891.1(CLASP1):c.196-670T>C	rs982261295
NM_001395891.1(CLASP1):c.[196-571C>T];[196-670T>G]

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.