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rs796052488

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052488(C;C)
Make rs796052488(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position161873129
GeneGABRA1
is asnp
is mentioned by
dbSNPrs796052488
ebirs796052488
HLIrs796052488
Exacrs796052488
Varsomers796052488
Maprs796052488
PheGenIrs796052488
hapmaprs796052488
1000 genomesrs796052488
hgdprs796052488
ensemblrs796052488
gopubmedrs796052488
geneviewrs796052488
scholarrs796052488
googlers796052488
pharmgkbrs796052488
gwascentralrs796052488
openSNPrs796052488
23andMers796052488
23andMe allrs796052488
SNP Nexus

SNPshotrs796052488
SNPdbers796052488
MSV3drs796052488
GWAS Ctlgrs796052488
Max Magnitude0
ClinVar
Risk rs796052488(C;C)
Alt rs796052488(C;C)
Reference rs796052488(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene GABRA1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.161300135G>C
CLNSRC
CLNACC RCV000187494.2,