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rs796052509

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052509(G;G)
Make rs796052509(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position162142313
GeneGABRG2
is asnp
is mentioned by
dbSNPrs796052509
ebirs796052509
HLIrs796052509
Exacrs796052509
Varsomers796052509
Maprs796052509
PheGenIrs796052509
hapmaprs796052509
1000 genomesrs796052509
hgdprs796052509
ensemblrs796052509
gopubmedrs796052509
geneviewrs796052509
scholarrs796052509
googlers796052509
pharmgkbrs796052509
gwascentralrs796052509
openSNPrs796052509
23andMers796052509
23andMe allrs796052509
SNP Nexus

SNPshotrs796052509
SNPdbers796052509
MSV3drs796052509
GWAS Ctlgrs796052509
Max Magnitude0
ClinVar
Risk rs796052509(G;G)
Alt rs796052509(G;G)
Reference rs796052509(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene GABRG2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.161569319T>G
CLNSRC
CLNACC RCV000187529.2,