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rs6917747

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs6917747(A;A)
Make rs6917747(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position159981673
GeneIGF2R
is asnp
is mentioned by
dbSNPrs6917747
ebirs6917747
HLIrs6917747
Exacrs6917747
Varsomers6917747
Maprs6917747
PheGenIrs6917747
hapmaprs6917747
1000 genomesrs6917747
hgdprs6917747
ensemblrs6917747
gopubmedrs6917747
geneviewrs6917747
scholarrs6917747
googlers6917747
pharmgkbrs6917747
gwascentralrs6917747
openSNPrs6917747
23andMers6917747
23andMe allrs6917747
SNP Nexus

SNPshotrs6917747
SNPdbers6917747
MSV3drs6917747
GWAS Ctlgrs6917747
GMAF0.07668
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19010793OA-icon.png]
Trait Brain lesion load
Title Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
Risk Allele
P-val 0.000007
Odds Ratio NR NR


[PMID 19307593OA-icon.png] Signals of recent positive selection in a worldwide sample of human populations.


GET Evidence
rs6917747
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.09375
summary