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rs794727962

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794727962(C;C)
Make rs794727962(C;T)
ReferenceGRCh38.p7 38.3/149
Chromosome5
Position161891045
GeneGABRA1
is asnp
is mentioned by
dbSNPrs794727962
dbSNP (classic)rs794727962
ClinGenrs794727962
ebirs794727962
HLIrs794727962
Exacrs794727962
Gnomadrs794727962
Varsomers794727962
LitVarrs794727962
Maprs794727962
PheGenIrs794727962
Biobankrs794727962
1000 genomesrs794727962
hgdprs794727962
ensemblrs794727962
geneviewrs794727962
scholarrs794727962
googlers794727962
pharmgkbrs794727962
gwascentralrs794727962
openSNPrs794727962
23andMers794727962
23andMe allrs794727962
SNPshotrs794727962
SNPdbers794727962
MSV3drs794727962
GWAS Ctlgrs794727962
Max Magnitude0
ClinVar
Risk rs794727962(C;C)
Alt rs794727962(C;C)
Reference Rs794727962(T;T)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene GABRA1
CLNDBN not provided not specified
Reversed 0
HGVS NC_000005.9:g.161318051T>C
CLNSRC
CLNACC RCV000180531.3, RCV000259148.1,