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rs730882211

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730882211(C;C)
Make rs730882211(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position118815132
GeneSEC24D
is asnp
is mentioned by
dbSNPrs730882211
ebirs730882211
HLIrs730882211
Exacrs730882211
Varsomers730882211
Maprs730882211
PheGenIrs730882211
hapmaprs730882211
1000 genomesrs730882211
hgdprs730882211
ensemblrs730882211
gopubmedrs730882211
geneviewrs730882211
scholarrs730882211
googlers730882211
pharmgkbrs730882211
gwascentralrs730882211
openSNPrs730882211
23andMers730882211
23andMe allrs730882211
SNP Nexus

SNPshotrs730882211
SNPdbers730882211
MSV3drs730882211
GWAS Ctlgrs730882211
Max Magnitude0
ClinVar
Risk rs730882211(C;C)
Alt rs730882211(C;C)
Reference rs730882211(G;G)
Significance Probable-Pathogenic
Disease Intellectual disability Seizures
Variation info
Gene SEC24D
CLNDBN Intellectual disability Seizures
Reversed 1
HGVS NC_000004.11:g.119736287C>G
CLNSRC
CLNACC RCV000162117.1,