rs1060501889

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs1060501889(-;-)

Make rs1060501889(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

5

Position

162149210

Gene

GABRG2

is a	snp
is	mentioned by
dbSNP	rs1060501889
dbSNP (classic)	rs1060501889
ClinGen	rs1060501889
ebi	rs1060501889
HLI	rs1060501889
Exac	rs1060501889
Gnomad	rs1060501889
Varsome	rs1060501889
LitVar	rs1060501889
Map	rs1060501889
PheGenI	rs1060501889
Biobank	rs1060501889
1000 genomes	rs1060501889
hgdp	rs1060501889
ensembl	rs1060501889
geneview	rs1060501889
scholar	rs1060501889
google	rs1060501889
pharmgkb	rs1060501889
gwascentral	rs1060501889
openSNP	rs1060501889
23andMe	rs1060501889
23andMe all	rs1060501889
SNPshot	rs1060501889
SNPdbe	rs1060501889
MSV3d	rs1060501889
GWAS Ctlg	rs1060501889

Max Magnitude

0

ClinVar
Risk	rs1060501889(-;-)
Alt	rs1060501889(-;-)
Reference	Rs1060501889(G;G)
Significance	Probable-Pathogenic
Disease	Epilepsy Familial febrile seizures 8
Variation	info
Gene	GABRG2
CLNDBN	Epilepsy, childhood absence 2 Familial febrile seizures 8
Reversed	0
HGVS	NC_000005.9:g.161576216delG
CLNSRC
CLNACC	RCV000462535.1,