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rs796052507

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052507(A;A)
Make rs796052507(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position162142163
GeneGABRG2
is asnp
is mentioned by
dbSNPrs796052507
ebirs796052507
HLIrs796052507
Exacrs796052507
Varsomers796052507
Maprs796052507
PheGenIrs796052507
hapmaprs796052507
1000 genomesrs796052507
hgdprs796052507
ensemblrs796052507
gopubmedrs796052507
geneviewrs796052507
scholarrs796052507
googlers796052507
pharmgkbrs796052507
gwascentralrs796052507
openSNPrs796052507
23andMers796052507
23andMe allrs796052507
SNP Nexus

SNPshotrs796052507
SNPdbers796052507
MSV3drs796052507
GWAS Ctlgrs796052507
Max Magnitude0
ClinVar
Risk rs796052507(A;A)
Alt rs796052507(A;A)
Reference rs796052507(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene GABRG2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.161569169G>A
CLNSRC
CLNACC RCV000187526.1,