List of variants in gene SYNE2 reported as benign by Eurofins NTD LLC (GA)

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: 36

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HGVS	dbSNP	gnomAD frequency
NM_182914.3(SYNE2):c.6481C>T (p.Leu2161=)	rs10151127	0.80823
NM_182914.3(SYNE2):c.20062-119G>C	rs1152588	0.66235
NM_182914.3(SYNE2):c.19333+5C>T	rs1152590	0.50736
NM_182914.3(SYNE2):c.1721T>C (p.Ile574Thr)	rs9944035	0.08879
NM_182914.3(SYNE2):c.12001T>C (p.Trp4001Arg)	rs2792205	0.08782
NM_182914.3(SYNE2):c.12002G>A (p.Trp4001Ter)	rs2781377	0.08740
NM_182914.3(SYNE2):c.7690A>G (p.Ile2564Val)	rs11628107	0.02936
NM_182914.3(SYNE2):c.12840+8T>C	rs145218296	0.02317
NM_182914.3(SYNE2):c.17561T>C (p.Leu5854Pro)	rs117070973	0.00528
NM_182914.3(SYNE2):c.12378C>T (p.Ser4126=)	rs36007735	0.00524
NM_182914.3(SYNE2):c.7162G>A (p.Glu2388Lys)	rs200842904	0.00462
NM_182914.3(SYNE2):c.6321C>T (p.Ser2107=)	rs143410137	0.00434
NM_182914.3(SYNE2):c.11379T>C (p.Leu3793=)	rs149391344	0.00319
NM_182914.3(SYNE2):c.20117G>A (p.Arg6706Gln)	rs35831865	0.00309
NM_182914.3(SYNE2):c.15781G>A (p.Val5261Ile)	rs144605670	0.00267
NM_182914.3(SYNE2):c.20410G>A (p.Asp6804Asn)	rs150644129	0.00259
NM_182914.3(SYNE2):c.12984A>G (p.Lys4328=)	rs151314114	0.00255
NM_182914.3(SYNE2):c.10835A>G (p.Gln3612Arg)	rs78110192	0.00249
NM_182914.3(SYNE2):c.19415C>T (p.Ser6472Leu)	rs150955173	0.00242
NM_182914.3(SYNE2):c.20382+9A>G	rs116394628	0.00230
NM_182914.3(SYNE2):c.20197G>A (p.Glu6733Lys)	rs150172232	0.00181
NM_182914.3(SYNE2):c.8041G>A (p.Val2681Ile)	rs150946074	0.00178
NM_182914.3(SYNE2):c.7898A>G (p.Asn2633Ser)	rs190582637	0.00157
NM_182914.3(SYNE2):c.9347A>G (p.Lys3116Arg)	rs138689053	0.00094
NM_182914.3(SYNE2):c.7124T>C (p.Leu2375Pro)	rs111902869	0.00091
NM_182914.3(SYNE2):c.12043T>C (p.Tyr4015His)	rs75665958	0.00029
NM_182914.3(SYNE2):c.7128A>G (p.Pro2376=)	rs117423703	0.00029
NM_182914.3(SYNE2):c.990+10A>G	rs145924910	0.00026
NM_182914.3(SYNE2):c.2013G>A (p.Leu671=)	rs371320284	0.00014
NM_182914.3(SYNE2):c.5608A>C (p.Ser1870Arg)	rs368227332	0.00001
NM_182914.3(SYNE2):c.9974C>T (p.Ala3325Val)	rs377173620	0.00001
NM_182914.3(SYNE2):c.1129-4dup	rs34440267
NM_182914.3(SYNE2):c.11944A>G (p.Asn3982Asp)	rs10137972
NM_182914.3(SYNE2):c.20339G>A (p.Arg6780Gln)	rs202240664
NM_182914.3(SYNE2):c.2070A>G (p.Leu690=)	rs79037871
NM_182914.3(SYNE2):c.2647-4_2647-3dup	rs397726340

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