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rs12410279

From SNPedia

Orientationplus
Stabilizedplus
Make rs12410279(A;A)
Make rs12410279(A;G)
Make rs12410279(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position220678178
is asnp
is mentioned by
dbSNPrs12410279
ebirs12410279
HLIrs12410279
Exacrs12410279
Varsomers12410279
Maprs12410279
PheGenIrs12410279
hapmaprs12410279
1000 genomesrs12410279
hgdprs12410279
ensemblrs12410279
gopubmedrs12410279
geneviewrs12410279
scholarrs12410279
googlers12410279
pharmgkbrs12410279
gwascentralrs12410279
openSNPrs12410279
23andMers12410279
23andMe allrs12410279
SNP Nexus

SNPshotrs12410279
SNPdbers12410279
MSV3drs12410279
GWAS Ctlgrs12410279
GMAF0.2112
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 18492799] Haplotype rs12740310*C-rs3737296*G-rs12410279*A was overtransmitted (p(corrected)=0.0016), with a relative risk for autism of 1.8 in homozygous carriers
OMIM606511
DescMAP/MICROTUBULE AFFINITY-REGULATING KINASE 1; MARK1
Variant
Relatedalso
OMIM610836
Desc
Variant
Relatedalso