List of variants in gene SYNE2 reported as uncertain significance by Genomic Research Center, Shahid Beheshti University of Medical Sciences

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_182914.3(SYNE2):c.14528T>A (p.Phe4843Tyr)	rs141488398	0.00042
NM_182914.3(SYNE2):c.11900T>G (p.Phe3967Cys)	rs1567266829
NM_182914.3(SYNE2):c.12037A>T (p.Asn4013Tyr)	rs1555478028
NM_182914.3(SYNE2):c.12609+1G>T	rs745516407
NM_182914.3(SYNE2):c.17557G>C (p.Glu5853Gln)	rs1158170304
NM_182914.3(SYNE2):c.20654C>G (p.Thr6885Ser)	rs1596340525
NM_182914.3(SYNE2):c.8272C>T (p.Pro2758Ser)	rs771389608

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