List of variants studied for psoriasis, susceptibility to

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 15

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_147686.4(TRAF3IP2):c.28G>A (p.Asp10Asn)	rs33980500	0.09825
NM_144701.3(IL23R):c.1142G>A (p.Arg381Gln)	rs11209026	0.04676
NM_144701.3(IL23R):c.491+17C>T	rs75363634	0.01464
NM_001039569.2(AP1S3):c.11T>G (p.Phe4Cys)	rs116107386	0.00898
NM_001039569.2(AP1S3):c.97C>T (p.Arg33Trp)	rs138292988	0.00726
NM_147686.4(TRAF3IP2):c.819C>G (p.His273Gln)	rs144405088	0.00172
NM_001039569.2(AP1S3):c.64A>G (p.Thr22Ala)	rs149183052	0.00125
NM_147686.4(TRAF3IP2):c.281G>A (p.Ser94Asn)	rs61756667	0.00110
NM_001039569.2(AP1S3):c.248T>C (p.Ile83Thr)	rs202157374	0.00002
NM_147686.4(TRAF3IP2):c.869T>G (p.Ile290Ser)	rs200074354	0.00002
NM_147686.4(TRAF3IP2):c.135C>G (p.Asn45Lys)	rs375324881	0.00001
HLA-C, HLA-Cw6
NM_144701.3(IL23R):c.492-9del	rs551451479
NM_147686.4(TRAF3IP2):c.1568G>C (p.Trp523Ser)	rs2536087765
NM_147686.4(TRAF3IP2):c.488_492del (p.Ser162_Leu163insTer)

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.