List of variants in gene GAD1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_000817.3(GAD1):c.-39A>C	rs45617531	0.00262
NM_000817.3(GAD1):c.1612-3A>G	rs113828797	0.00179
NM_000817.3(GAD1):c.1473T>C (p.Tyr491=)	rs146199288	0.00168
NM_000817.3(GAD1):c.1173C>T (p.Asn391=)	rs34856125	0.00094
NM_000817.3(GAD1):c.1251C>T (p.Leu417=)	rs35426017	0.00094
NM_000817.3(GAD1):c.807G>A (p.Pro269=)	rs34100397	0.00094
NM_000817.3(GAD1):c.1611+5G>A	rs147201199	0.00070
NM_000817.3(GAD1):c.1002+4T>G	rs139531653	0.00060
NM_000817.3(GAD1):c.399T>C (p.Asp133=)	rs112737041	0.00058
NM_000817.3(GAD1):c.682A>C (p.Ile228Leu)	rs45566933	0.00040
NM_000817.3(GAD1):c.1773C>A (p.Gly591=)	rs202061730	0.00020
NM_000817.3(GAD1):c.1224C>T (p.Gly408=)
NM_000817.3(GAD1):c.1252G>T (p.Val418Phe)	rs143058194
NM_000817.3(GAD1):c.1476C>G (p.Ala492=)
NM_000817.3(GAD1):c.260G>A (p.Arg87His)
NM_000817.3(GAD1):c.354G>A (p.Leu118=)
NM_000817.3(GAD1):c.59A>G (p.Asn20Ser)
NM_000817.3(GAD1):c.750T>C (p.Pro250=)
NM_000817.3(GAD1):c.822G>A (p.Lys274=)

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