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rs864321707

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864321707(C;T)
Make rs864321707(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63439608
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs864321707
ebirs864321707
HLIrs864321707
Exacrs864321707
Varsomers864321707
Maprs864321707
PheGenIrs864321707
hapmaprs864321707
1000 genomesrs864321707
hgdprs864321707
ensemblrs864321707
gopubmedrs864321707
geneviewrs864321707
scholarrs864321707
googlers864321707
pharmgkbrs864321707
gwascentralrs864321707
openSNPrs864321707
23andMers864321707
23andMe allrs864321707
SNP Nexus

SNPshotrs864321707
SNPdbers864321707
MSV3drs864321707
GWAS Ctlgrs864321707
Max Magnitude0
ClinVar
Risk rs864321707(T;T)
Alt rs864321707(T;T)
Reference rs864321707(C;C)
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.62070961G>A
CLNSRC
CLNACC RCV000203598.1,