List of variants in gene GABRG2 reported 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
		ClinVar version:

Total variants: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_198904.4(GABRG2):c.588C>T (p.Asn196=)	rs211037	0.31659
NM_198904.4(GABRG2):c.798T>C (p.Phe266=)	rs115126975	0.00067
NM_198904.4(GABRG2):c.1320G>A (p.Gly440=)	rs150727562	0.00020
NM_198904.4(GABRG2):c.768C>T (p.Ser256=)	rs201672465	0.00015
NM_198904.4(GABRG2):c.582G>A (p.Leu194=)	rs781498456	0.00002
NM_198904.4(GABRG2):c.691G>A (p.Asp231Asn)	rs773065895	0.00002
NM_198904.4(GABRG2):c.1000G>A (p.Ala334Thr)	rs398123523	0.00001
NM_198904.4(GABRG2):c.1110T>C (p.Asp370=)	rs201824364	0.00001
NM_198904.4(GABRG2):c.1113_1115del (p.Lys374del)	rs727503941

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.