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rs796052636

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052636(A;A)
Make rs796052636(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63439681
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052636
ebirs796052636
HLIrs796052636
Exacrs796052636
Varsomers796052636
Maprs796052636
PheGenIrs796052636
hapmaprs796052636
1000 genomesrs796052636
hgdprs796052636
ensemblrs796052636
gopubmedrs796052636
geneviewrs796052636
scholarrs796052636
googlers796052636
pharmgkbrs796052636
gwascentralrs796052636
openSNPrs796052636
23andMers796052636
23andMe allrs796052636
SNP Nexus

SNPshotrs796052636
SNPdbers796052636
MSV3drs796052636
GWAS Ctlgrs796052636
Max Magnitude0
ClinVar
Risk rs796052636(A;A)
Alt rs796052636(A;A)
Reference rs796052636(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62071034C>T
CLNSRC
CLNACC RCV000187881.2,