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rs117067974

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs117067974(C;G)
Make rs117067974(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position63414174
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs117067974
ebirs117067974
HLIrs117067974
Exacrs117067974
Varsomers117067974
Maprs117067974
PheGenIrs117067974
hapmaprs117067974
1000 genomesrs117067974
hgdprs117067974
ensemblrs117067974
gopubmedrs117067974
geneviewrs117067974
scholarrs117067974
googlers117067974
pharmgkbrs117067974
gwascentralrs117067974
openSNPrs117067974
23andMers117067974
23andMe allrs117067974
SNP Nexus

SNPshotrs117067974
SNPdbers117067974
MSV3drs117067974
GWAS Ctlgrs117067974
GMAF0.0101
Max Magnitude0
ClinVar
Risk rs117067974(A,G;A,G)
Alt rs117067974(A,G;A,G)
Reference rs117067974(C;C)
Significance Other
Disease Benign familial neonatal seizures 1 not specified
Variation info
Gene KCNQ2
CLNDBN Benign familial neonatal seizures 1 not specified
Reversed 0
HGVS NC_000020.10:g.62045527C>G
CLNSRC ClinVar GeneDx GeneReviews University of Chicago
CLNACC RCV000020972.1, RCV000117341.3,


OMIM121200
Desc
Variant
Relatedalso