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rs796052504

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052504(C;T)
Make rs796052504(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position162097716
GeneGABRG2
is asnp
is mentioned by
dbSNPrs796052504
ebirs796052504
HLIrs796052504
Exacrs796052504
Varsomers796052504
Maprs796052504
PheGenIrs796052504
hapmaprs796052504
1000 genomesrs796052504
hgdprs796052504
ensemblrs796052504
gopubmedrs796052504
geneviewrs796052504
scholarrs796052504
googlers796052504
pharmgkbrs796052504
gwascentralrs796052504
openSNPrs796052504
23andMers796052504
23andMe allrs796052504
SNP Nexus

SNPshotrs796052504
SNPdbers796052504
MSV3drs796052504
GWAS Ctlgrs796052504
Max Magnitude0
ClinVar
Risk rs796052504(T;T)
Alt rs796052504(T;T)
Reference rs796052504(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene GABRG2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.161524722C>T
CLNSRC
CLNACC RCV000187521.1,