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rs796052505

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052505(A;A)
Make rs796052505(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position162095551
GeneGABRG2
is asnp
is mentioned by
dbSNPrs796052505
ebirs796052505
HLIrs796052505
Exacrs796052505
Varsomers796052505
Maprs796052505
PheGenIrs796052505
hapmaprs796052505
1000 genomesrs796052505
hgdprs796052505
ensemblrs796052505
gopubmedrs796052505
geneviewrs796052505
scholarrs796052505
googlers796052505
pharmgkbrs796052505
gwascentralrs796052505
openSNPrs796052505
23andMers796052505
23andMe allrs796052505
SNP Nexus

SNPshotrs796052505
SNPdbers796052505
MSV3drs796052505
GWAS Ctlgrs796052505
Max Magnitude0
ClinVar
Risk rs796052505(A;A)
Alt rs796052505(A;A)
Reference rs796052505(G;G)
Significance Other
Disease not provided
Variation info
Gene GABRG2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.161522557G>A
CLNSRC
CLNACC RCV000187522.3,