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rs796052513

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052513(C;T)
Make rs796052513(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position162153237
GeneGABRG2
is asnp
is mentioned by
dbSNPrs796052513
ebirs796052513
HLIrs796052513
Exacrs796052513
Varsomers796052513
Maprs796052513
PheGenIrs796052513
hapmaprs796052513
1000 genomesrs796052513
hgdprs796052513
ensemblrs796052513
gopubmedrs796052513
geneviewrs796052513
scholarrs796052513
googlers796052513
pharmgkbrs796052513
gwascentralrs796052513
openSNPrs796052513
23andMers796052513
23andMe allrs796052513
SNP Nexus

SNPshotrs796052513
SNPdbers796052513
MSV3drs796052513
GWAS Ctlgrs796052513
Max Magnitude0
ClinVar
Risk rs796052513(T;T)
Alt rs796052513(T;T)
Reference rs796052513(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene GABRG2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.161580243C>T
CLNSRC
CLNACC RCV000187536.1,