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rs796052497

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052497(C;G)
Make rs796052497(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position161895700
GeneGABRA1
is asnp
is mentioned by
dbSNPrs796052497
ebirs796052497
HLIrs796052497
Exacrs796052497
Varsomers796052497
Maprs796052497
PheGenIrs796052497
hapmaprs796052497
1000 genomesrs796052497
hgdprs796052497
ensemblrs796052497
gopubmedrs796052497
geneviewrs796052497
scholarrs796052497
googlers796052497
pharmgkbrs796052497
gwascentralrs796052497
openSNPrs796052497
23andMers796052497
23andMe allrs796052497
SNP Nexus

SNPshotrs796052497
SNPdbers796052497
MSV3drs796052497
GWAS Ctlgrs796052497
Max Magnitude0
ClinVar
Risk rs796052497(G;G)
Alt rs796052497(G;G)
Reference rs796052497(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GABRA1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.161322706C>G
CLNSRC
CLNACC RCV000187505.2,