rs768061156

Orientation

plus

Stabilized

plus

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

Make rs768061156(G;T)

Make rs768061156(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

5

Position

162149170

Gene

GABRG2

is a	snp
is	mentioned by
dbSNP	rs768061156
dbSNP (classic)	rs768061156
ClinGen	rs768061156
ebi	rs768061156
HLI	rs768061156
Exac	rs768061156
Gnomad	rs768061156
Varsome	rs768061156
LitVar	rs768061156
Map	rs768061156
PheGenI	rs768061156
Biobank	rs768061156
1000 genomes	rs768061156
hgdp	rs768061156
ensembl	rs768061156
geneview	rs768061156
scholar	rs768061156
google	rs768061156
pharmgkb	rs768061156
gwascentral	rs768061156
openSNP	rs768061156
23andMe	rs768061156
SNPshot	rs768061156
SNPdbe	rs768061156
MSV3d	rs768061156
GWAS Ctlg	rs768061156

Max Magnitude

0

ClinVar
Risk	rs768061156(T;T)
Alt	rs768061156(T;T)
Reference	Rs768061156(G;G)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	GABRG2
CLNDBN	not specified
Reversed	0
HGVS	NC_000005.9:g.161576176G>T
CLNSRC
CLNACC	RCV000187532.3,