List of variants in gene HSPB8 reported as uncertain significance for Charcot-Marie-Tooth disease

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: 4

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HGVS	dbSNP
NM_014365.2(HSPB8):c.422A>C (p.Lys141Thr)	rs1565929090
NM_014365.2(HSPB8):c.423G>T (p.Lys141Asn)	rs104894345
NM_014365.3(HSPB8):c.25T>C (p.Ser9Pro)	rs774233360
NM_014365.3(HSPB8):c.506C>T (p.Pro169Leu)	rs1592932892

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