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rs1005573

From SNPedia

Orientationplus
Stabilizedplus
Make rs1005573(C;C)
Make rs1005573(C;T)
Make rs1005573(T;T)
ReferenceGRCh38.p7 38.3/151
Chromosome21
Position33026408
GeneOLIG2
is asnp
is mentioned by
dbSNPrs1005573
dbSNP (classic)rs1005573
ClinGenrs1005573
ebirs1005573
HLIrs1005573
Exacrs1005573
Gnomadrs1005573
Varsomers1005573
LitVarrs1005573
Maprs1005573
PheGenIrs1005573
Biobankrs1005573
1000 genomesrs1005573
hgdprs1005573
ensemblrs1005573
geneviewrs1005573
scholarrs1005573
googlers1005573
pharmgkbrs1005573
gwascentralrs1005573
openSNPrs1005573
23andMers1005573
23andMe allrs1005573
SNPshotrs1005573
SNPdbers1005573
MSV3drs1005573
GWAS Ctlgrs1005573
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 30178266] Variants of the OLIG2 Gene are Associated with Cerebral Palsy in Chinese Han Infants with Hypoxic-Ischemic Encephalopathy.