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rs876657400

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657400(A;A)
Make rs876657400(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position11025812
GeneSLC6A1
is asnp
is mentioned by
dbSNPrs876657400
ebirs876657400
HLIrs876657400
Exacrs876657400
Varsomers876657400
Maprs876657400
PheGenIrs876657400
hapmaprs876657400
1000 genomesrs876657400
hgdprs876657400
ensemblrs876657400
gopubmedrs876657400
geneviewrs876657400
scholarrs876657400
googlers876657400
pharmgkbrs876657400
gwascentralrs876657400
openSNPrs876657400
23andMers876657400
23andMe allrs876657400
SNP Nexus

SNPshotrs876657400
SNPdbers876657400
MSV3drs876657400
GWAS Ctlgrs876657400
Max Magnitude0
ClinVar
Risk rs876657400(A;A)
Alt rs876657400(A;A)
Reference rs876657400(G;G)
Significance Pathogenic
Disease Myoclonic-atonic epilepsy
Variation info
Gene SLC6A1
CLNDBN Myoclonic-atonic epilepsy
Reversed 0
HGVS NC_000003.11:g.11067498G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000172995.2,