Have questions? Visit https://www.reddit.com/r/SNPedia

rs281864926

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281864926(G;G)
Make rs281864926(G;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position20630721
GeneSLC6A5
is asnp
is mentioned by
dbSNPrs281864926
ebirs281864926
HLIrs281864926
Exacrs281864926
Varsomers281864926
Maprs281864926
PheGenIrs281864926
hapmaprs281864926
1000 genomesrs281864926
hgdprs281864926
ensemblrs281864926
gopubmedrs281864926
geneviewrs281864926
scholarrs281864926
googlers281864926
pharmgkbrs281864926
gwascentralrs281864926
openSNPrs281864926
23andMers281864926
23andMe allrs281864926
SNP Nexus

SNPshotrs281864926
SNPdbers281864926
MSV3drs281864926
GWAS Ctlgrs281864926
Max Magnitude0
ClinVar
Risk rs281864926(G;G)
Alt rs281864926(G;G)
Reference rs281864926(T;T)
Significance Pathogenic
Disease Hyperekplexia 3
Variation info
Gene SLC6A5
CLNDBN Hyperekplexia 3
Reversed 0
HGVS NC_000011.9:g.20652267T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000024247.4,