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rs587777861

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777861(C;C)
Make rs587777861(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position128220016
GeneDNM1
is asnp
is mentioned by
dbSNPrs587777861
ebirs587777861
HLIrs587777861
Exacrs587777861
Varsomers587777861
Maprs587777861
PheGenIrs587777861
hapmaprs587777861
1000 genomesrs587777861
hgdprs587777861
ensemblrs587777861
gopubmedrs587777861
geneviewrs587777861
scholarrs587777861
googlers587777861
pharmgkbrs587777861
gwascentralrs587777861
openSNPrs587777861
23andMers587777861
23andMe allrs587777861
SNP Nexus

SNPshotrs587777861
SNPdbers587777861
MSV3drs587777861
GWAS Ctlgrs587777861
Max Magnitude0
ClinVar
Risk rs587777861(C;C)
Alt rs587777861(C;C)
Reference rs587777861(G;G)
Significance Pathogenic
Disease Epileptic encephalopathy
Variation info
Gene DNM1
CLNDBN Epileptic encephalopathy, early infantile, 31
Reversed 0
HGVS NC_000009.11:g.130982295G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000144708.7,