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rs12518194

From SNPedia

Orientationplus
Stabilizedplus
Make rs12518194(A;A)
Make rs12518194(A;G)
Make rs12518194(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position25951452
is asnp
is mentioned by
dbSNPrs12518194
ebirs12518194
HLIrs12518194
Exacrs12518194
Varsomers12518194
Maprs12518194
PheGenIrs12518194
hapmaprs12518194
1000 genomesrs12518194
hgdprs12518194
ensemblrs12518194
gopubmedrs12518194
geneviewrs12518194
scholarrs12518194
googlers12518194
pharmgkbrs12518194
gwascentralrs12518194
openSNPrs12518194
23andMers12518194
23andMe allrs12518194
SNP Nexus

SNPshotrs12518194
SNPdbers12518194
MSV3drs12518194
GWAS Ctlgrs12518194
GMAF0.2369
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19456320OA-icon.png] A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.


GET Evidence
rs12518194
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.226562
summary