List of variants reported as uncertain significance for Hypoproteinemia, hypercatabolic; Amyloidosis, hereditary systemic 6

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Total variants: 8

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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.164T>C (p.Ile55Thr)
NM_004048.4(B2M):c.275C>T (p.Pro92Leu)
NM_004048.4(B2M):c.32C>T (p.Ala11Val)
NM_004048.4(B2M):c.37C>T (p.Leu13Phe)
NM_004048.4(B2M):c.67C>T (p.Arg23Cys)

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