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rs796052642

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052642(A;A)
Make rs796052642(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position63438639
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs796052642
ebirs796052642
HLIrs796052642
Exacrs796052642
Varsomers796052642
Maprs796052642
PheGenIrs796052642
hapmaprs796052642
1000 genomesrs796052642
hgdprs796052642
ensemblrs796052642
gopubmedrs796052642
geneviewrs796052642
scholarrs796052642
googlers796052642
pharmgkbrs796052642
gwascentralrs796052642
openSNPrs796052642
23andMers796052642
23andMe allrs796052642
SNP Nexus

SNPshotrs796052642
SNPdbers796052642
MSV3drs796052642
GWAS Ctlgrs796052642
Max Magnitude0
ClinVar
Risk rs796052642(A;A)
Alt rs796052642(A;A)
Reference rs796052642(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62069992C>T
CLNSRC
CLNACC RCV000187890.2,