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

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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.340A>C (p.Lys114Gln)	rs372078625	0.00011
NM_004048.4(B2M):c.278C>A (p.Thr93Asn)	rs778103494	0.00002
NM_004048.4(B2M):c.160G>A (p.Asp54Asn)	rs148494241	0.00001
NM_004048.4(B2M):c.50G>A (p.Gly17Asp)	rs1196771735	0.00001
NM_004048.4(B2M):c.5C>T (p.Ser2Phe)	rs368160918	0.00001
NC_000015.9:g.(?_45007601)_(45008540_?)dup
NM_004048.4(B2M):c.106G>A (p.Glu36Lys)	rs1204151497
NM_004048.4(B2M):c.135C>G (p.Cys45Trp)
NM_004048.4(B2M):c.154_155delinsTT (p.Pro52Leu)	rs2141288680
NM_004048.4(B2M):c.245T>C (p.Phe82Ser)
NM_004048.4(B2M):c.278C>T (p.Thr93Ile)
NM_004048.4(B2M):c.301C>T (p.Arg101Cys)
NM_004048.4(B2M):c.313G>A (p.Val105Met)	rs2086933060
NM_004048.4(B2M):c.31G>C (p.Ala11Pro)	rs104894481
NM_004048.4(B2M):c.355A>G (p.Met119Val)
NM_004048.4(B2M):c.358T>C (p.Ter120Gln)
NM_004048.4(B2M):c.52C>G (p.Leu18Val)
NM_004048.4(B2M):c.61A>G (p.Ile21Val)	rs757230673
NM_004048.4(B2M):c.7C>T (p.Arg3Cys)	rs765817584
NM_004048.4(B2M):c.85G>T (p.Val29Phe)	rs1304731273
NM_004048.4(B2M):c.8G>A (p.Arg3His)
NM_004048.4(B2M):c.94C>T (p.Arg32Cys)

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