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rs10431386

From SNPedia

Orientationplus
Stabilizedplus
Make rs10431386(C;C)
Make rs10431386(C;T)
Make rs10431386(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position120691123
GeneMLEC
is asnp
is mentioned by
dbSNPrs10431386
dbSNP (classic)rs10431386
ClinGenrs10431386
ebirs10431386
HLIrs10431386
Exacrs10431386
Gnomadrs10431386
Varsomers10431386
LitVarrs10431386
Maprs10431386
PheGenIrs10431386
Biobankrs10431386
1000 genomesrs10431386
hgdprs10431386
ensemblrs10431386
geneviewrs10431386
scholarrs10431386
googlers10431386
pharmgkbrs10431386
gwascentralrs10431386
openSNPrs10431386
23andMers10431386
SNPshotrs10431386
SNPdbers10431386
MSV3drs10431386
GWAS Ctlgrs10431386
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 28972276] MLEC gene polymorphisms promote cerebral palsy via M2-like macrophage polarization.