Have questions? Visit https://www.reddit.com/r/SNPedia

rs796052496

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052496(C;T)
Make rs796052496(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position161895693
GeneGABRA1
is asnp
is mentioned by
dbSNPrs796052496
ebirs796052496
HLIrs796052496
Exacrs796052496
Varsomers796052496
Maprs796052496
PheGenIrs796052496
hapmaprs796052496
1000 genomesrs796052496
hgdprs796052496
ensemblrs796052496
gopubmedrs796052496
geneviewrs796052496
scholarrs796052496
googlers796052496
pharmgkbrs796052496
gwascentralrs796052496
openSNPrs796052496
23andMers796052496
23andMe allrs796052496
SNP Nexus

SNPshotrs796052496
SNPdbers796052496
MSV3drs796052496
GWAS Ctlgrs796052496
Max Magnitude0
ClinVar
Risk rs796052496(T;T)
Alt rs796052496(T;T)
Reference rs796052496(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene GABRA1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.161322699C>T
CLNSRC
CLNACC RCV000187504.2,