List of variants in gene SYNE2 reported as likely benign by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

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.18039-5T>A	rs189611387	0.00199
NM_182914.3(SYNE2):c.19964A>T (p.Gln6655Leu)	rs149978500	0.00193
NM_182914.3(SYNE2):c.12572G>A (p.Gly4191Asp)	rs145227848	0.00094
NM_182914.3(SYNE2):c.4178G>A (p.Arg1393Gln)	rs117647282	0.00064
NM_182914.3(SYNE2):c.10494A>G (p.Thr3498=)	rs201000414	0.00058
NM_182914.3(SYNE2):c.4912T>C (p.Tyr1638His)	rs146801942	0.00052
NM_182914.3(SYNE2):c.12370G>T (p.Val4124Leu)	rs370255444	0.00019

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