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rs2229944

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2229944(C;T)
Make rs2229944(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position161294312
GeneGABRB2
is asnp
is mentioned by
dbSNPrs2229944
dbSNP (old)rs2229944
ClinGenrs2229944
ebirs2229944
HLIrs2229944
Exacrs2229944
Gnomadrs2229944
Varsomers2229944
Maprs2229944
PheGenIrs2229944
Biobankrs2229944
1000 genomesrs2229944
hgdprs2229944
ensemblrs2229944
gopubmedrs2229944
geneviewrs2229944
scholarrs2229944
googlers2229944
pharmgkbrs2229944
gwascentralrs2229944
openSNPrs2229944
23andMers2229944
23andMe allrs2229944
SNP Nexus

SNPshotrs2229944
SNPdbers2229944
MSV3drs2229944
GWAS Ctlgrs2229944
GMAF0.1088
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 20404824] Imprinting in the schizophrenia candidate gene GABRB2 encoding GABA(A) receptor beta(2) subunit


ClinVar
Risk rs2229944(T;T)
Alt rs2229944(T;T)
Reference Rs2229944(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene GABRB2
CLNDBN not specified
Reversed 1
HGVS NC_000005.9:g.160721319G>A
CLNSRC
CLNACC RCV000429656.1,