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rs398122856

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398122856(G;G)
Make rs398122856(G;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position157136872
GeneGLRB
is asnp
is mentioned by
dbSNPrs398122856
ebirs398122856
HLIrs398122856
Exacrs398122856
Varsomers398122856
Maprs398122856
PheGenIrs398122856
hapmaprs398122856
1000 genomesrs398122856
hgdprs398122856
ensemblrs398122856
gopubmedrs398122856
geneviewrs398122856
scholarrs398122856
googlers398122856
pharmgkbrs398122856
gwascentralrs398122856
openSNPrs398122856
23andMers398122856
23andMe allrs398122856
SNP Nexus

SNPshotrs398122856
SNPdbers398122856
MSV3drs398122856
GWAS Ctlgrs398122856
Max Magnitude0
ClinVar
Risk rs398122856(G;G)
Alt rs398122856(G;G)
Reference rs398122856(T;T)
Significance Pathogenic
Disease Hyperekplexia 2
Variation info
Gene GLRB
CLNDBN Hyperekplexia 2
Reversed 0
HGVS NC_000004.11:g.158058024T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000024246.27,