List of variants in gene TSC2 reported as uncertain significance by Gharavi Laboratory, Columbia University

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000548.5(TSC2):c.3145G>A (p.Glu1049Lys)	rs796053492	0.00003
NM_000548.5(TSC2):c.1678G>A (p.Val560Met)	rs141631268	0.00001
NM_000548.5(TSC2):c.1585G>T (p.Asp529Tyr)	rs1567438280
NM_000548.5(TSC2):c.1724T>C (p.Leu575Pro)	rs1567456901
NM_000548.5(TSC2):c.2218A>G (p.Met740Val)	rs757345150
NM_000548.5(TSC2):c.3137C>T (p.Pro1046Leu)	rs1567497682
NM_000548.5(TSC2):c.4008_4010del (p.Ser1338del)	rs1567520255
NM_000548.5(TSC2):c.5042A>G (p.Asn1681Ser)	rs1567128450
NM_000548.5(TSC2):c.5230C>T (p.Leu1744Phe)	rs1567132207

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