ClinVar Miner

List of variants in gene FCGR2B reported as risk factor for lupus erythematosus

Included ClinVar conditions (16):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001394477.1(FCGR2B):c.695T>C (p.Ile232Thr)	rs1050501	0.19240
NM_004001.4(FCGR2B):c.-386G>C	rs3219018

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