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rs796052506

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052506(A;G)
Make rs796052506(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position162097729
GeneGABRG2
is asnp
is mentioned by
dbSNPrs796052506
ebirs796052506
HLIrs796052506
Exacrs796052506
Varsomers796052506
Maprs796052506
PheGenIrs796052506
hapmaprs796052506
1000 genomesrs796052506
hgdprs796052506
ensemblrs796052506
gopubmedrs796052506
geneviewrs796052506
scholarrs796052506
googlers796052506
pharmgkbrs796052506
gwascentralrs796052506
openSNPrs796052506
23andMers796052506
23andMe allrs796052506
SNP Nexus

SNPshotrs796052506
SNPdbers796052506
MSV3drs796052506
GWAS Ctlgrs796052506
Max Magnitude0
ClinVar
Risk rs796052506(G;G)
Alt rs796052506(G;G)
Reference rs796052506(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GABRG2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.161524735A>G
CLNSRC
CLNACC RCV000187523.2,