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rs769404

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs769404(C;C)
Make rs769404(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position170822115
GeneGAD1
is asnp
is mentioned by
dbSNPrs769404
dbSNP (classic)rs769404
ClinGenrs769404
ebirs769404
HLIrs769404
Exacrs769404
Gnomadrs769404
Varsomers769404
LitVarrs769404
Maprs769404
PheGenIrs769404
Biobankrs769404
1000 genomesrs769404
hgdprs769404
ensemblrs769404
geneviewrs769404
scholarrs769404
googlers769404
pharmgkbrs769404
gwascentralrs769404
openSNPrs769404
23andMers769404
SNPshotrs769404
SNPdbers769404
MSV3drs769404
GWAS Ctlgrs769404
Merged fromRs11542313
GMAF0.3646
Max Magnitude0
ClinVar
Risk rs769404(C;C)
Alt rs769404(C;C)
Reference Rs769404(T;T)
Significance Non-pathogenic
Disease Cerebral palsy spastic quadriplegic
Variation info
Gene GAD1
CLNDBN Cerebral palsy spastic quadriplegic
Reversed 0
HGVS NC_000002.11:g.171678625T>C
CLNSRC
CLNACC RCV000368065.1,