rs796052506

Orientation

plus

Stabilized

plus

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

Make rs796052506(A;G)

Make rs796052506(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

5

Position

162097729

Gene

GABRG2

is a	snp
is	mentioned by
dbSNP	rs796052506
ClinGen	rs796052506
ebi	rs796052506
HLI	rs796052506
Exac	rs796052506
Varsome	rs796052506
Map	rs796052506
PheGenI	rs796052506
hapmap	rs796052506
1000 genomes	rs796052506
hgdp	rs796052506
ensembl	rs796052506
gopubmed	rs796052506
geneview	rs796052506
scholar	rs796052506
google	rs796052506
pharmgkb	rs796052506
gwascentral	rs796052506
openSNP	rs796052506
23andMe	rs796052506
23andMe all	rs796052506
SNP Nexus
SNPshot	rs796052506
SNPdbe	rs796052506
MSV3d	rs796052506
GWAS Ctlg	rs796052506

Max Magnitude

0

ClinVar
Risk	rs796052506(G;G)
Alt	rs796052506(G;G)
Reference	Rs796052506(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GABRG2
CLNDBN	not provided
Reversed	0
HGVS	NC_000005.9:g.161524735A>G
CLNSRC
CLNACC	RCV000187523.2,