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rs717947

From SNPedia

Orientationminus
Stabilizedminus
Make rs717947(A;A)
Make rs717947(A;G)
Make rs717947(G;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position33652135
is asnp
is mentioned by
dbSNPrs717947
ebirs717947
HLIrs717947
Exacrs717947
Varsomers717947
Maprs717947
PheGenIrs717947
hapmaprs717947
1000 genomesrs717947
hgdprs717947
ensemblrs717947
gopubmedrs717947
geneviewrs717947
scholarrs717947
googlers717947
pharmgkbrs717947
gwascentralrs717947
openSNPrs717947
23andMers717947
23andMe allrs717947
SNP Nexus

SNPshotrs717947
SNPdbers717947
MSV3drs717947
GWAS Ctlgrs717947
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 25988933] A genome-wide identified risk variant for PTSD is a methylation quantitative trait locus and confers decreased cortical activation to fearful faces