List of variants reported as uncertain significance for Ritscher-Schinzel syndrome 1

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_014846.4(WASHC5):c.2422A>G (p.Ile808Val)	rs144507279	0.00024
NM_014846.4(WASHC5):c.2257C>T (p.Arg753Cys)	rs780719370	0.00003
NM_014846.4(WASHC5):c.625G>A (p.Glu209Lys)	rs565980279	0.00002
NM_014846.4(WASHC5):c.872G>A (p.Ser291Asn)	rs753529606	0.00001
NM_014846.4(WASHC5):c.1102_1103del (p.Asp368fs)
NM_014846.4(WASHC5):c.1133T>G (p.Leu378Arg)	rs758822672
NM_014846.4(WASHC5):c.1136A>G (p.His379Arg)
NM_014846.4(WASHC5):c.2429A>T (p.Lys810Met)	rs780468544
NM_014846.4(WASHC5):c.2849A>G (p.Lys950Arg)	rs1815967070
NM_014846.4(WASHC5):c.2954+3_2954+4delinsCG
NM_020134.4(DPYSL5):c.139G>A (p.Gly47Arg)	rs1558337060

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.