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rs886039375

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039375(G;T)
Make rs886039375(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome5
Position161331051
GeneGABRB2
is asnp
is mentioned by
dbSNPrs886039375
dbSNP (classic)rs886039375
ClinGenrs886039375
ebirs886039375
HLIrs886039375
Exacrs886039375
Gnomadrs886039375
Varsomers886039375
LitVarrs886039375
Maprs886039375
PheGenIrs886039375
Biobankrs886039375
1000 genomesrs886039375
hgdprs886039375
ensemblrs886039375
geneviewrs886039375
scholarrs886039375
googlers886039375
pharmgkbrs886039375
gwascentralrs886039375
openSNPrs886039375
23andMers886039375
SNPshotrs886039375
SNPdbers886039375
MSV3drs886039375
GWAS Ctlgrs886039375
Max Magnitude0
ClinVar
Risk rs886039375(T;T)
Alt rs886039375(T;T)
Reference Rs886039375(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GABRB2
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.160758058C>A
CLNSRC
CLNACC RCV000255464.1,