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rs772800738

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs772800738(C;C)
Make rs772800738(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63433878
GeneKCNQ2, LOC105372721
is asnp
is mentioned by
dbSNPrs772800738
ebirs772800738
HLIrs772800738
Exacrs772800738
Varsomers772800738
Maprs772800738
PheGenIrs772800738
hapmaprs772800738
1000 genomesrs772800738
hgdprs772800738
ensemblrs772800738
gopubmedrs772800738
geneviewrs772800738
scholarrs772800738
googlers772800738
pharmgkbrs772800738
gwascentralrs772800738
openSNPrs772800738
23andMers772800738
23andMe allrs772800738
SNP Nexus

SNPshotrs772800738
SNPdbers772800738
MSV3drs772800738
GWAS Ctlgrs772800738
Max Magnitude0
ClinVar
Risk rs772800738(C;C)
Alt rs772800738(C;C)
Reference rs772800738(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.62065231T>A
CLNSRC
CLNACC RCV000187894.1,