rs796052504

Orientation

plus

Stabilized

plus

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

Make rs796052504(C;T)

Make rs796052504(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

162097716

Gene

GABRG2

is a	snp
is	mentioned by
dbSNP	rs796052504
ClinGen	rs796052504
ebi	rs796052504
HLI	rs796052504
Exac	rs796052504
Varsome	rs796052504
Map	rs796052504
PheGenI	rs796052504
hapmap	rs796052504
1000 genomes	rs796052504
hgdp	rs796052504
ensembl	rs796052504
gopubmed	rs796052504
geneview	rs796052504
scholar	rs796052504
google	rs796052504
pharmgkb	rs796052504
gwascentral	rs796052504
openSNP	rs796052504
23andMe	rs796052504
23andMe all	rs796052504
SNP Nexus
SNPshot	rs796052504
SNPdbe	rs796052504
MSV3d	rs796052504
GWAS Ctlg	rs796052504

Max Magnitude

0

ClinVar
Risk	rs796052504(T;T)
Alt	rs796052504(T;T)
Reference	Rs796052504(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	GABRG2
CLNDBN	not provided
Reversed	0
HGVS	NC_000005.9:g.161524722C>T
CLNSRC
CLNACC	RCV000187521.1,