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

rs1057521979

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057521979(C;C)
Make rs1057521979(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position161411034
GeneGABRB2
is asnp
is mentioned by
dbSNPrs1057521979
dbSNP (old)rs1057521979
ClinGenrs1057521979
ebirs1057521979
HLIrs1057521979
Exacrs1057521979
Gnomadrs1057521979
Varsomers1057521979
Maprs1057521979
PheGenIrs1057521979
Biobankrs1057521979
1000 genomesrs1057521979
hgdprs1057521979
ensemblrs1057521979
gopubmedrs1057521979
geneviewrs1057521979
scholarrs1057521979
googlers1057521979
pharmgkbrs1057521979
gwascentralrs1057521979
openSNPrs1057521979
23andMers1057521979
23andMe allrs1057521979
SNPshotrs1057521979
SNPdbers1057521979
MSV3drs1057521979
GWAS Ctlgrs1057521979
Max Magnitude0
ClinVar
Risk rs1057521979(C;C)
Alt rs1057521979(C;C)
Reference Rs1057521979(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GABRB2
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.160838040A>G
CLNSRC
CLNACC RCV000439405.1,