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rs796052503

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052503(C;G)
Make rs796052503(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position162093940
GeneGABRG2
is asnp
is mentioned by
dbSNPrs796052503
ebirs796052503
HLIrs796052503
Exacrs796052503
Varsomers796052503
Maprs796052503
PheGenIrs796052503
hapmaprs796052503
1000 genomesrs796052503
hgdprs796052503
ensemblrs796052503
gopubmedrs796052503
geneviewrs796052503
scholarrs796052503
googlers796052503
pharmgkbrs796052503
gwascentralrs796052503
openSNPrs796052503
23andMers796052503
23andMe allrs796052503
SNP Nexus

SNPshotrs796052503
SNPdbers796052503
MSV3drs796052503
GWAS Ctlgrs796052503
Max Magnitude0
ClinVar
Risk rs796052503(G;G)
Alt rs796052503(G;G)
Reference rs796052503(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GABRG2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.161520946C>G
CLNSRC
CLNACC RCV000187519.1,