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rs874628

From SNPedia

Orientationminus
Stabilizedminus
Make rs874628(C;C)
Make rs874628(C;T)
Make rs874628(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position18193890
GeneMPV17L2
is asnp
is mentioned by
dbSNPrs874628
ebirs874628
HLIrs874628
Exacrs874628
Varsomers874628
Maprs874628
PheGenIrs874628
hapmaprs874628
1000 genomesrs874628
hgdprs874628
ensemblrs874628
gopubmedrs874628
geneviewrs874628
scholarrs874628
googlers874628
pharmgkbrs874628
gwascentralrs874628
openSNPrs874628
23andMers874628
23andMe allrs874628
SNP Nexus

SNPshotrs874628
SNPdbers874628
MSV3drs874628
GWAS Ctlgrs874628
GMAF0.1919
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21833088OA-icon.png]
Trait
Title Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Risk Allele A
P-val 1E-8
Odds Ratio 1.1100 [1.09-1.12]


[PMID 15752431OA-icon.png] Association between a variation in the phosphodiesterase 4D gene and bone mineral density.


[PMID 16584842] Variants in the RAB3A gene are not associated with mental retardation in the Chinese population.


[PMID 20405052OA-icon.png] The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.


GET Evidence
MPV17L2-M72V
aa_change Met72Val
aa_change_short M72V
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.246625
summary