Have questions? Visit https://www.reddit.com/r/SNPedia

rs796052518

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052518(G;G)
Make rs796052518(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position162095507
GeneGABRG2
is asnp
is mentioned by
dbSNPrs796052518
ebirs796052518
HLIrs796052518
Exacrs796052518
Varsomers796052518
Maprs796052518
PheGenIrs796052518
hapmaprs796052518
1000 genomesrs796052518
hgdprs796052518
ensemblrs796052518
gopubmedrs796052518
geneviewrs796052518
scholarrs796052518
googlers796052518
pharmgkbrs796052518
gwascentralrs796052518
openSNPrs796052518
23andMers796052518
23andMe allrs796052518
SNP Nexus

SNPshotrs796052518
SNPdbers796052518
MSV3drs796052518
GWAS Ctlgrs796052518
Max Magnitude0
ClinVar
Risk rs796052518(G;G)
Alt rs796052518(G;G)
Reference rs796052518(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene GABRG2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.161522513T>G
CLNSRC
CLNACC RCV000187544.1,