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rs796052667

From SNPedia

Orientationminus
Make rs796052667(-;-)
Make rs796052667(-;CT)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63407136
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052667
ebirs796052667
HLIrs796052667
Exacrs796052667
Varsomers796052667
Maprs796052667
PheGenIrs796052667
hapmaprs796052667
1000 genomesrs796052667
hgdprs796052667
ensemblrs796052667
gopubmedrs796052667
geneviewrs796052667
scholarrs796052667
googlers796052667
pharmgkbrs796052667
gwascentralrs796052667
openSNPrs796052667
23andMers796052667
23andMe allrs796052667
SNP Nexus

SNPshotrs796052667
SNPdbers796052667
MSV3drs796052667
GWAS Ctlgrs796052667
Max Magnitude
ClinVar
Risk rs796052667(;)
Alt rs796052667(;)
Reference rs796052667(CT;CT)
Significance Pathogenic
Disease not provided Inborn genetic diseases
Variation info
Gene KCNQ2
CLNDBN not provided Inborn genetic diseases
Reversed 1
HGVS NC_000020.10:g.62038489_62038490delAG
CLNSRC
CLNACC RCV000187947.1, RCV000190798.1,