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rs71651682

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs71651682(C;T)
Make rs71651682(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position26772759
GeneGABRB3
is asnp
is mentioned by
dbSNPrs71651682
ebirs71651682
HLIrs71651682
Exacrs71651682
Varsomers71651682
Maprs71651682
PheGenIrs71651682
hapmaprs71651682
1000 genomesrs71651682
hgdprs71651682
ensemblrs71651682
gopubmedrs71651682
geneviewrs71651682
scholarrs71651682
googlers71651682
pharmgkbrs71651682
gwascentralrs71651682
openSNPrs71651682
23andMers71651682
23andMe allrs71651682
SNP Nexus

SNPshotrs71651682
SNPdbers71651682
MSV3drs71651682
GWAS Ctlgrs71651682
Max Magnitude0
OMIM137192
Desc
Variant0004
Relatedalso
ClinVar
Risk rs71651682(T;T)
Alt rs71651682(T;T)
Reference rs71651682(C;C)
Significance Other
Disease Epilepsy
Variation info
Gene GABRB3
CLNDBN Epilepsy, childhood absence 5
Reversed 0
HGVS NC_000015.9:g.27017906C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017577.2,