Have questions? Visit https://www.reddit.com/r/SNPedia

rs716595

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs716595(A;A)
Make rs716595(A;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position110246728
GeneMXI1
is asnp
is mentioned by
dbSNPrs716595
ebirs716595
HLIrs716595
Exacrs716595
Varsomers716595
Maprs716595
PheGenIrs716595
hapmaprs716595
1000 genomesrs716595
hgdprs716595
ensemblrs716595
gopubmedrs716595
geneviewrs716595
scholarrs716595
googlers716595
pharmgkbrs716595
gwascentralrs716595
openSNPrs716595
23andMers716595
23andMe allrs716595
SNP Nexus

SNPshotrs716595
SNPdbers716595
MSV3drs716595
GWAS Ctlgrs716595
GMAF0.1483
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19010793OA-icon.png]
Trait Normalized brain volume
Title Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
Risk Allele
P-val 0.000008
Odds Ratio NR NR



GET Evidence
rs716595
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.132812
summary