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rs796052632

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052632(A;A)
Make rs796052632(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63442432
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052632
ebirs796052632
HLIrs796052632
Exacrs796052632
Varsomers796052632
Maprs796052632
PheGenIrs796052632
hapmaprs796052632
1000 genomesrs796052632
hgdprs796052632
ensemblrs796052632
gopubmedrs796052632
geneviewrs796052632
scholarrs796052632
googlers796052632
pharmgkbrs796052632
gwascentralrs796052632
openSNPrs796052632
23andMers796052632
23andMe allrs796052632
SNP Nexus

SNPshotrs796052632
SNPdbers796052632
MSV3drs796052632
GWAS Ctlgrs796052632
Max Magnitude0
ClinVar
Risk rs796052632(A;A)
Alt rs796052632(A;A)
Reference rs796052632(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62073785A>T
CLNSRC
CLNACC RCV000187874.2,