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rs786205232

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205232(A;A)
Make rs786205232(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position110603893
GeneKCNA2
is asnp
is mentioned by
dbSNPrs786205232
ebirs786205232
HLIrs786205232
Exacrs786205232
Varsomers786205232
Maprs786205232
PheGenIrs786205232
hapmaprs786205232
1000 genomesrs786205232
hgdprs786205232
ensemblrs786205232
gopubmedrs786205232
geneviewrs786205232
scholarrs786205232
googlers786205232
pharmgkbrs786205232
gwascentralrs786205232
openSNPrs786205232
23andMers786205232
23andMe allrs786205232
SNP Nexus

SNPshotrs786205232
SNPdbers786205232
MSV3drs786205232
GWAS Ctlgrs786205232
Max Magnitude0
ClinVar
Risk rs786205232(A;A)
Alt rs786205232(A;A)
Reference rs786205232(G;G)
Significance Pathogenic
Disease Epileptic encephalopathy
Variation info
Gene KCNA2
CLNDBN Epileptic encephalopathy, early infantile, 32
Reversed 1
HGVS NC_000001.10:g.111146515C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000170514.4,