List of variants reported as benign for STT3B-congenital disorder of glycosylation by Invitae

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_178862.3(STT3B):c.778-17C>A	rs11705765	0.05239
NM_178862.3(STT3B):c.777+7T>G	rs76400963	0.01303
NM_178862.3(STT3B):c.2406C>A (p.Thr802=)	rs17027884	0.01283
NM_178862.3(STT3B):c.477A>G (p.Thr159=)	rs139496568	0.01086
NM_178862.3(STT3B):c.1764C>T (p.Tyr588=)	rs34176522	0.00770
NM_178862.3(STT3B):c.1172+15A>G	rs60153256	0.00288
NM_178862.3(STT3B):c.372T>C (p.Asn124=)	rs150886803	0.00245
NM_178862.3(STT3B):c.2073+14T>C	rs59520046	0.00143
NM_178862.3(STT3B):c.2322A>G (p.Ala774=)	rs140420950	0.00109
NM_178862.3(STT3B):c.2401-17G>T	rs370120522	0.00041
NM_178862.3(STT3B):c.136G>A (p.Gly46Ser)	rs527396203	0.00026
NM_178862.3(STT3B):c.141C>T (p.Gly47=)	rs367626371	0.00019
NM_178862.3(STT3B):c.2401-5dup

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