List of variants in gene STAT1 reported as likely pathogenic for autoimmune disease

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: 19

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_007315.4(STAT1):c.1066T>G (p.Tyr356Asp)
NM_007315.4(STAT1):c.1127+1G>A
NM_007315.4(STAT1):c.1128-1G>A
NM_007315.4(STAT1):c.1166T>G (p.Val389Gly)	rs1692876152
NM_007315.4(STAT1):c.1198C>G (p.Leu400Val)
NM_007315.4(STAT1):c.1210T>G (p.Phe404Val)
NM_007315.4(STAT1):c.1632+1G>A
NM_007315.4(STAT1):c.2102A>G (p.Tyr701Cys)	rs2124996723
NM_007315.4(STAT1):c.2135+2T>A	rs2124996603
NM_007315.4(STAT1):c.511G>A (p.Asp171Asn)	rs2125075054
NM_007315.4(STAT1):c.511G>C (p.Asp171His)
NM_007315.4(STAT1):c.516C>G (p.Phe172Leu)
NM_007315.4(STAT1):c.820C>G (p.Arg274Gly)	rs387906758
NM_007315.4(STAT1):c.851A>G (p.Glu284Gly)	rs1693752801
NM_007315.4(STAT1):c.856A>C (p.Lys286Gln)	rs1693752377
NM_007315.4(STAT1):c.865T>C (p.Tyr289His)
NM_007315.4(STAT1):c.876C>A (p.Asp292Glu)	rs1085307649
NM_007315.4(STAT1):c.970T>C (p.Cys324Arg)	rs1574653439
NM_007315.4(STAT1):c.974T>A (p.Met325Lys)

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.