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rs796052627

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052627(A;A)
Make rs796052627(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63444713
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052627
ebirs796052627
HLIrs796052627
Exacrs796052627
Varsomers796052627
Maprs796052627
PheGenIrs796052627
hapmaprs796052627
1000 genomesrs796052627
hgdprs796052627
ensemblrs796052627
gopubmedrs796052627
geneviewrs796052627
scholarrs796052627
googlers796052627
pharmgkbrs796052627
gwascentralrs796052627
openSNPrs796052627
23andMers796052627
23andMe allrs796052627
SNP Nexus

SNPshotrs796052627
SNPdbers796052627
MSV3drs796052627
GWAS Ctlgrs796052627
Max Magnitude0
ClinVar
Risk rs796052627(A;A)
Alt rs796052627(A;A)
Reference rs796052627(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62076066G>T
CLNSRC
CLNACC RCV000187865.2,