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rs796052643

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052643(C;G)
Make rs796052643(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63438638
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052643
ebirs796052643
HLIrs796052643
Exacrs796052643
Varsomers796052643
Maprs796052643
PheGenIrs796052643
hapmaprs796052643
1000 genomesrs796052643
hgdprs796052643
ensemblrs796052643
gopubmedrs796052643
geneviewrs796052643
scholarrs796052643
googlers796052643
pharmgkbrs796052643
gwascentralrs796052643
openSNPrs796052643
23andMers796052643
23andMe allrs796052643
SNP Nexus

SNPshotrs796052643
SNPdbers796052643
MSV3drs796052643
GWAS Ctlgrs796052643
Max Magnitude0
ClinVar
Risk rs796052643(G;G)
Alt rs796052643(G;G)
Reference rs796052643(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62069991G>C
CLNSRC
CLNACC RCV000187891.2,