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rs759584387

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs759584387(A;A)
Make rs759584387(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63413556
GeneKCNQ2, LOC105372724
is asnp
is mentioned by
dbSNPrs759584387
ebirs759584387
HLIrs759584387
Exacrs759584387
Varsomers759584387
Maprs759584387
PheGenIrs759584387
hapmaprs759584387
1000 genomesrs759584387
hgdprs759584387
ensemblrs759584387
gopubmedrs759584387
geneviewrs759584387
scholarrs759584387
googlers759584387
pharmgkbrs759584387
gwascentralrs759584387
openSNPrs759584387
23andMers759584387
23andMe allrs759584387
SNP Nexus

SNPshotrs759584387
SNPdbers759584387
MSV3drs759584387
GWAS Ctlgrs759584387
Max Magnitude0
ClinVar
Risk rs759584387(A,T;A,T)
Alt rs759584387(A,T;A,T)
Reference rs759584387(G;G)
Significance Pathogenic
Disease not provided Benign familial neonatal seizures 1
Variation info
Gene KCNQ2
CLNDBN not provided Benign familial neonatal seizures 1
Reversed 0
HGVS NC_000020.10:g.62044909G>A
CLNSRC
CLNACC RCV000187912.1, RCV000203596.1,