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rs730882225

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730882225(A;A)
Make rs730882225(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position235980495
GeneNID1
is asnp
is mentioned by
dbSNPrs730882225
ebirs730882225
HLIrs730882225
Exacrs730882225
Varsomers730882225
Maprs730882225
PheGenIrs730882225
hapmaprs730882225
1000 genomesrs730882225
hgdprs730882225
ensemblrs730882225
gopubmedrs730882225
geneviewrs730882225
scholarrs730882225
googlers730882225
pharmgkbrs730882225
gwascentralrs730882225
openSNPrs730882225
23andMers730882225
23andMe allrs730882225
SNP Nexus

SNPshotrs730882225
SNPdbers730882225
MSV3drs730882225
GWAS Ctlgrs730882225
Max Magnitude0
ClinVar
Risk rs730882225(A;A)
Alt rs730882225(A;A)
Reference rs730882225(G;G)
Significance Probable-Pathogenic
Disease Focal epilepsy Hemiparesis Hydrocephalus
Variation info
Gene NID1
CLNDBN Focal epilepsy Hemiparesis Hydrocephalus
Reversed 1
HGVS NC_000001.10:g.236143795C>T
CLNSRC
CLNACC RCV000162140.1,