List of variants in gene GABRG2 reported as likely benign by Ambry Genetics

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_198904.4(GABRG2):c.954C>T (p.Leu318=)	rs749531013	0.00025
NM_198904.4(GABRG2):c.1320G>A (p.Gly440=)	rs150727562	0.00020
NM_198904.4(GABRG2):c.1236C>T (p.Tyr412=)	rs749951528	0.00018
NM_198904.4(GABRG2):c.11C>T (p.Pro4Leu)	rs375295110	0.00014
NM_198904.4(GABRG2):c.243T>A (p.Leu81=)	rs143295869	0.00014
NM_198904.4(GABRG2):c.1356T>C (p.Tyr452=)	rs762386331	0.00009
NM_198904.4(GABRG2):c.36A>T (p.Ser12=)	rs762058667	0.00006
NM_198904.4(GABRG2):c.1189A>G (p.Ile397Val)	rs375785093	0.00004
NM_198904.4(GABRG2):c.219G>A (p.Leu73=)	rs753076158	0.00004
NM_198904.4(GABRG2):c.942A>G (p.Thr314=)	rs377502016	0.00004
NM_198904.4(GABRG2):c.1413C>T (p.Ser471=)	rs765926862	0.00001
NM_198904.4(GABRG2):c.372A>T (p.Arg124Ser)	rs754884716	0.00001
NM_198904.4(GABRG2):c.789T>G (p.Ser263=)	rs754514348	0.00001
NM_198904.4(GABRG2):c.-4del	rs771282908
NM_198904.4(GABRG2):c.1314A>G (p.Arg438=)
NM_198904.4(GABRG2):c.150T>C (p.Ala50=)	rs1264403667
NM_198904.4(GABRG2):c.840T>C (p.Tyr280=)	rs558779533
NM_198904.4(GABRG2):c.843C>A (p.Ile281=)	rs749127891

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