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rs4141463

From SNPedia

Orientationplus
Stabilizedplus
Make rs4141463(C;C)
Make rs4141463(C;T)
Make rs4141463(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position14766825
GeneMACROD2
is asnp
is mentioned by
dbSNPrs4141463
ebirs4141463
HLIrs4141463
Exacrs4141463
Varsomers4141463
Maprs4141463
PheGenIrs4141463
hapmaprs4141463
1000 genomesrs4141463
hgdprs4141463
ensemblrs4141463
gopubmedrs4141463
geneviewrs4141463
scholarrs4141463
googlers4141463
pharmgkbrs4141463
gwascentralrs4141463
openSNPrs4141463
23andMers4141463
23andMe allrs4141463
SNP Nexus

SNPshotrs4141463
SNPdbers4141463
MSV3drs4141463
GWAS Ctlgrs4141463
GMAF0.3875
Max Magnitude
rs4141463 is a SNP within an intron of the MACROD2 gene.

A 2010 study by the Autism Genome Project of 1,558 "rigorously defined" autism spectrum disorder families found some - but slight - evidence for an association between rs4141463 and risk for autism.[PMID 20663923OA-icon.png]

However, an independent case-control study published in 2011 of 1,170 cases of autism spectrum disorder patients failed to replicate any association between autism risk and rs4141463.[PMID 21656903]

? (C;C) (C;T) (T;T) 28


[PMID 22739633] The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families