rs121434580

Orientation

plus

Stabilized

plus

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

Make rs121434580(A;C)

Make rs121434580(C;C)

Reference

GRCh38 38.1/141

Chromosome

1

Position

2027636

Gene

GABRD

is a	snp
is	mentioned by
dbSNP	rs121434580
dbSNP (classic)	rs121434580
ClinGen	rs121434580
ebi	rs121434580
HLI	rs121434580
Exac	rs121434580
Gnomad	rs121434580
Varsome	rs121434580
LitVar	rs121434580
Map	rs121434580
PheGenI	rs121434580
Biobank	rs121434580
1000 genomes	rs121434580
hgdp	rs121434580
ensembl	rs121434580
geneview	rs121434580
scholar	rs121434580
google	rs121434580
pharmgkb	rs121434580
gwascentral	rs121434580
openSNP	rs121434580
23andMe	rs121434580
SNPshot	rs121434580
SNPdbe	rs121434580
MSV3d	rs121434580
GWAS Ctlg	rs121434580

Max Magnitude

0

OMIM	137163
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121434580(C;C)
Alt	rs121434580(C;C)
Reference	Rs121434580(A;A)
Significance	Other
Disease	Generalized epilepsy with febrile seizures plus type 5
Variation	info
Gene	GABRD
CLNDBN	Generalized epilepsy with febrile seizures plus type 5
Reversed	0
HGVS	NC_000001.10:g.1959075A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017598.2,