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rs4150167

From SNPedia

Orientationminus
Stabilizedplus
Make rs4150167(A;A)
Make rs4150167(A;G)
Make rs4150167(G;G)
ReferenceGRCh38 38.1/142
Chromosome16
Position84180078
GeneTAF1C
is asnp
is mentioned by
dbSNPrs4150167
ebirs4150167
HLIrs4150167
Exacrs4150167
Varsomers4150167
Maprs4150167
PheGenIrs4150167
hapmaprs4150167
1000 genomesrs4150167
hgdprs4150167
ensemblrs4150167
gopubmedrs4150167
geneviewrs4150167
scholarrs4150167
googlers4150167
pharmgkbrs4150167
gwascentralrs4150167
openSNPrs4150167
23andMers4150167
23andMe allrs4150167
SNP Nexus

SNPshotrs4150167
SNPdbers4150167
MSV3drs4150167
GWAS Ctlgrs4150167
GMAF0.008724
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22843504OA-icon.png]
Trait Autism
Title Individual common variants exert weak effects on the risk for autism spectrum disorderspi.
Risk Allele
P-val 3E-7
Odds Ratio 1.96 [1.52-2.56]


[PMID 16400609OA-icon.png] Single-nucleotide polymorphisms in NAGNAG acceptors are highly predictive for variations of alternative splicing.