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rs796052635

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052635(A;A)
Make rs796052635(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63439707
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052635
ebirs796052635
HLIrs796052635
Exacrs796052635
Varsomers796052635
Maprs796052635
PheGenIrs796052635
hapmaprs796052635
1000 genomesrs796052635
hgdprs796052635
ensemblrs796052635
gopubmedrs796052635
geneviewrs796052635
scholarrs796052635
googlers796052635
pharmgkbrs796052635
gwascentralrs796052635
openSNPrs796052635
23andMers796052635
23andMe allrs796052635
SNP Nexus

SNPshotrs796052635
SNPdbers796052635
MSV3drs796052635
GWAS Ctlgrs796052635
Max Magnitude0
ClinVar
Risk rs796052635(A;A)
Alt rs796052635(A;A)
Reference rs796052635(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62071060A>T
CLNSRC
CLNACC RCV000187880.1,