List of variants in gene combination ADAT3, SCAMP4 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
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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_138422.4(ADAT3):c.117G>A (p.Pro39=)	rs199915192	0.00342
NM_138422.4(ADAT3):c.216C>G (p.Thr72=)	rs140122850	0.00282
NM_138422.4(ADAT3):c.831C>T (p.Arg277=)	rs142175228	0.00282
NM_138422.4(ADAT3):c.383G>T (p.Arg128Leu)	rs200992550	0.00230
NM_138422.4(ADAT3):c.111T>G (p.Pro37=)	rs760510020	0.00021
NM_138422.4(ADAT3):c.444G>A (p.Pro148=)	rs937114381	0.00006
NM_138422.4(ADAT3):c.147C>T (p.Ser49=)
NM_138422.4(ADAT3):c.165C>T (p.Asp55=)
NM_138422.4(ADAT3):c.867C>T (p.Asp289=)

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