rs796052513

Orientation

plus

Stabilized

plus

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

Make rs796052513(C;T)

Make rs796052513(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

162153237

Gene

GABRG2

is a	snp
is	mentioned by
dbSNP	rs796052513
dbSNP (classic)	rs796052513
ClinGen	rs796052513
ebi	rs796052513
HLI	rs796052513
Exac	rs796052513
Gnomad	rs796052513
Varsome	rs796052513
LitVar	rs796052513
Map	rs796052513
PheGenI	rs796052513
Biobank	rs796052513
1000 genomes	rs796052513
hgdp	rs796052513
ensembl	rs796052513
geneview	rs796052513
scholar	rs796052513
google	rs796052513
pharmgkb	rs796052513
gwascentral	rs796052513
openSNP	rs796052513
23andMe	rs796052513
SNPshot	rs796052513
SNPdbe	rs796052513
MSV3d	rs796052513
GWAS Ctlg	rs796052513

Max Magnitude

0

ClinVar
Risk	rs796052513(T;T)
Alt	rs796052513(T;T)
Reference	Rs796052513(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	GABRG2
CLNDBN	not provided
Reversed	0
HGVS	NC_000005.9:g.161580243C>T
CLNSRC
CLNACC	RCV000187536.1,