ClinVar Miner

List of variants in gene B2M reported as pathogenic for Hypoproteinemia, hypercatabolic

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)
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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_004048.4(B2M):c.20T>A (p.Leu7Ter)
NM_004048.4(B2M):c.31G>C (p.Ala11Pro)	rs104894481
NM_004048.4(B2M):c.67+1G>T	rs863225287

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