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rs796052508

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052508(A;A)
Make rs796052508(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position162142238
GeneGABRG2
is asnp
is mentioned by
dbSNPrs796052508
ebirs796052508
HLIrs796052508
Exacrs796052508
Varsomers796052508
Maprs796052508
PheGenIrs796052508
hapmaprs796052508
1000 genomesrs796052508
hgdprs796052508
ensemblrs796052508
gopubmedrs796052508
geneviewrs796052508
scholarrs796052508
googlers796052508
pharmgkbrs796052508
gwascentralrs796052508
openSNPrs796052508
23andMers796052508
23andMe allrs796052508
SNP Nexus

SNPshotrs796052508
SNPdbers796052508
MSV3drs796052508
GWAS Ctlgrs796052508
Max Magnitude0
ClinVar
Risk rs796052508(A,T;A,T)
Alt rs796052508(A,T;A,T)
Reference rs796052508(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene GABRG2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.161569244C>A; NC_000005.9:g.161569244C>T
CLNSRC
CLNACC RCV000187527.2, RCV000187528.1,