List of variants in gene SOCS1 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_003745.2(SOCS1):c.368C>G (p.Pro123Arg)	rs1244284678
NM_003745.2(SOCS1):c.460T>C (p.Tyr154His)	rs2069578995
NM_003745.2(SOCS1):c.476_480dup (p.Met161fs)	rs1470306246

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