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rs864321706

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864321706(G;G)
Make rs864321706(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63439675
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs864321706
ebirs864321706
HLIrs864321706
Exacrs864321706
Varsomers864321706
Maprs864321706
PheGenIrs864321706
hapmaprs864321706
1000 genomesrs864321706
hgdprs864321706
ensemblrs864321706
gopubmedrs864321706
geneviewrs864321706
scholarrs864321706
googlers864321706
pharmgkbrs864321706
gwascentralrs864321706
openSNPrs864321706
23andMers864321706
23andMe allrs864321706
SNP Nexus

SNPshotrs864321706
SNPdbers864321706
MSV3drs864321706
GWAS Ctlgrs864321706
Max Magnitude0
ClinVar
Risk rs864321706(G;G)
Alt rs864321706(G;G)
Reference rs864321706(T;T)
Significance Pathogenic
Disease Early infantile epileptic encephalopathy 7
Variation info
Gene KCNQ2
CLNDBN Early infantile epileptic encephalopathy 7
Reversed 1
HGVS NC_000020.10:g.62071028A>C
CLNSRC
CLNACC RCV000203589.1,