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rs796052628

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052628(C;C)
Make rs796052628(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63444678
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052628
ebirs796052628
HLIrs796052628
Exacrs796052628
Varsomers796052628
Maprs796052628
PheGenIrs796052628
hapmaprs796052628
1000 genomesrs796052628
hgdprs796052628
ensemblrs796052628
gopubmedrs796052628
geneviewrs796052628
scholarrs796052628
googlers796052628
pharmgkbrs796052628
gwascentralrs796052628
openSNPrs796052628
23andMers796052628
23andMe allrs796052628
SNP Nexus

SNPshotrs796052628
SNPdbers796052628
MSV3drs796052628
GWAS Ctlgrs796052628
Max Magnitude0
ClinVar
Risk rs796052628(C;C)
Alt rs796052628(C;C)
Reference rs796052628(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62076031A>G
CLNSRC
CLNACC RCV000187869.1,