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rs730882060

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730882060(-;-)
Make rs730882060(-;GGGCC)
Make rs730882060(GGGCC;GGGCC)
ReferenceGRCh38.p2 38.2/144
Chromosome20
Position63406653
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs730882060
ebirs730882060
HLIrs730882060
Exacrs730882060
Varsomers730882060
Maprs730882060
PheGenIrs730882060
hapmaprs730882060
1000 genomesrs730882060
hgdprs730882060
ensemblrs730882060
gopubmedrs730882060
geneviewrs730882060
scholarrs730882060
googlers730882060
pharmgkbrs730882060
gwascentralrs730882060
openSNPrs730882060
23andMers730882060
23andMe allrs730882060
SNP Nexus

SNPshotrs730882060
SNPdbers730882060
MSV3drs730882060
GWAS Ctlgrs730882060
Max Magnitude0
ClinVar
Risk rs730882060(GGGCC;GGGCC)
Alt rs730882060(GGGCC;GGGCC)
Reference rs730882060(;)
Significance Pathogenic
Disease Benign familial neonatal seizures 1
Variation info
Gene KCNQ2
CLNDBN Benign familial neonatal seizures 1
Reversed 1
HGVS NC_000020.10:g.62038007_62038011dupGGCCC
CLNSRC
CLNACC RCV000020990.1,