List of variants in gene B2M reported as likely benign 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)
		ClinVar version:

Total variants: 22

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HGVS	dbSNP	gnomAD frequency
NM_004048.4(B2M):c.68-13C>T	rs149900092	0.00032
NM_004048.4(B2M):c.159C>T (p.Ser53=)	rs200164063	0.00016
NM_004048.4(B2M):c.279T>C (p.Thr93=)	rs766309912	0.00005
NM_004048.4(B2M):c.68-12G>A	rs375970981	0.00003
NM_004048.4(B2M):c.168A>G (p.Glu56=)	rs1347307081	0.00001
NM_004048.4(B2M):c.33G>C (p.Ala11=)	rs781314311	0.00001
NM_004048.4(B2M):c.67+12C>T	rs771780544	0.00001
NM_004048.4(B2M):c.114A>G (p.Gly38=)
NM_004048.4(B2M):c.126C>T (p.Phe42=)
NM_004048.4(B2M):c.147G>A (p.Gly49=)
NM_004048.4(B2M):c.147G>T (p.Gly49=)	rs768464174
NM_004048.4(B2M):c.156A>C (p.Pro52=)
NM_004048.4(B2M):c.24T>C (p.Ala8=)
NM_004048.4(B2M):c.27G>A (p.Val9=)
NM_004048.4(B2M):c.300C>T (p.Cys100=)
NM_004048.4(B2M):c.306G>A (p.Val102=)
NM_004048.4(B2M):c.312T>C (p.His104=)
NM_004048.4(B2M):c.347-15C>T
NM_004048.4(B2M):c.347-4A>G	rs2086941192
NM_004048.4(B2M):c.67+20C>A
NM_004048.4(B2M):c.67+20C>T
NM_004048.4(B2M):c.68-10T>C	rs2141288465

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