rs267606837

Orientation

plus

Stabilized

plus

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

Make rs267606837(C;G)

Make rs267606837(G;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

162097839

Gene

GABRG2

is a	snp
is	mentioned by
dbSNP	rs267606837
dbSNP (classic)	rs267606837
ClinGen	rs267606837
ebi	rs267606837
HLI	rs267606837
Exac	rs267606837
Gnomad	rs267606837
Varsome	rs267606837
LitVar	rs267606837
Map	rs267606837
PheGenI	rs267606837
Biobank	rs267606837
1000 genomes	rs267606837
hgdp	rs267606837
ensembl	rs267606837
geneview	rs267606837
scholar	rs267606837
google	rs267606837
pharmgkb	rs267606837
gwascentral	rs267606837
openSNP	rs267606837
23andMe	rs267606837
SNPshot	rs267606837
SNPdbe	rs267606837
MSV3d	rs267606837
GWAS Ctlg	rs267606837

Max Magnitude

0

ClinVar
Risk	rs267606837(G;G)
Alt	rs267606837(G;G)
Reference	Rs267606837(C;C)
Significance	Pathogenic
Disease	Familial febrile seizures 8
Variation	info
Gene	GABRG2
CLNDBN	Familial febrile seizures 8
Reversed	0
HGVS	NC_000005.9:g.161524845C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017597.28,