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rs796052519

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052519(A;A)
Make rs796052519(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position162095516
GeneGABRG2
is asnp
is mentioned by
dbSNPrs796052519
ebirs796052519
HLIrs796052519
Exacrs796052519
Varsomers796052519
Maprs796052519
PheGenIrs796052519
hapmaprs796052519
1000 genomesrs796052519
hgdprs796052519
ensemblrs796052519
gopubmedrs796052519
geneviewrs796052519
scholarrs796052519
googlers796052519
pharmgkbrs796052519
gwascentralrs796052519
openSNPrs796052519
23andMers796052519
23andMe allrs796052519
SNP Nexus

SNPshotrs796052519
SNPdbers796052519
MSV3drs796052519
GWAS Ctlgrs796052519
Max Magnitude0
ClinVar
Risk rs796052519(A;A)
Alt rs796052519(A;A)
Reference rs796052519(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GABRG2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.161522522C>A
CLNSRC
CLNACC RCV000187545.1,