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rs766755499

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs766755499(C;C)
Make rs766755499(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63407326
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs766755499
ebirs766755499
HLIrs766755499
Exacrs766755499
Varsomers766755499
Maprs766755499
PheGenIrs766755499
hapmaprs766755499
1000 genomesrs766755499
hgdprs766755499
ensemblrs766755499
gopubmedrs766755499
geneviewrs766755499
scholarrs766755499
googlers766755499
pharmgkbrs766755499
gwascentralrs766755499
openSNPrs766755499
23andMers766755499
23andMe allrs766755499
SNP Nexus

SNPshotrs766755499
SNPdbers766755499
MSV3drs766755499
GWAS Ctlgrs766755499
Max Magnitude0
ClinVar
Risk rs766755499(C;C)
Alt rs766755499(C;C)
Reference rs766755499(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.62038679T>C
CLNSRC
CLNACC RCV000187927.2,