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rs796052495

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052495(C;T)
Make rs796052495(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position161895690
GeneGABRA1
is asnp
is mentioned by
dbSNPrs796052495
ebirs796052495
HLIrs796052495
Exacrs796052495
Varsomers796052495
Maprs796052495
PheGenIrs796052495
hapmaprs796052495
1000 genomesrs796052495
hgdprs796052495
ensemblrs796052495
gopubmedrs796052495
geneviewrs796052495
scholarrs796052495
googlers796052495
pharmgkbrs796052495
gwascentralrs796052495
openSNPrs796052495
23andMers796052495
23andMe allrs796052495
SNP Nexus

SNPshotrs796052495
SNPdbers796052495
MSV3drs796052495
GWAS Ctlgrs796052495
Max Magnitude0
ClinVar
Risk rs796052495(T;T)
Alt rs796052495(T;T)
Reference rs796052495(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GABRA1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.161322696C>T
CLNSRC
CLNACC RCV000187503.1,