rs121909673

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common genotype

Make rs121909673(A;A)

Make rs121909673(A;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

162093965

Gene

GABRG2

is a	snp
is	mentioned by
dbSNP	rs121909673
dbSNP (classic)	rs121909673
ClinGen	rs121909673
ebi	rs121909673
HLI	rs121909673
Exac	rs121909673
Gnomad	rs121909673
Varsome	rs121909673
LitVar	rs121909673
Map	rs121909673
PheGenI	rs121909673
Biobank	rs121909673
1000 genomes	rs121909673
hgdp	rs121909673
ensembl	rs121909673
geneview	rs121909673
scholar	rs121909673
google	rs121909673
pharmgkb	rs121909673
gwascentral	rs121909673
openSNP	rs121909673
23andMe	rs121909673
SNPshot	rs121909673
SNPdbe	rs121909673
MSV3d	rs121909673
GWAS Ctlg	rs121909673

Merged from

Rs28933070

Max Magnitude

0

OMIM	137164
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121909673(A;A)
Alt	rs121909673(A;A)
Reference	Rs121909673(G;G)
Significance	Other
Disease	Epilepsy Familial febrile seizures 8 not provided
Variation	info
Gene	GABRG2
CLNDBN	Epilepsy, childhood absence 2 Familial febrile seizures 8 not provided
Reversed	0
HGVS	NC_000005.9:g.161520971G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017592.4, RCV000017593.29, RCV000187520.2,