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rs11808092

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs11808092(A;A)
Make rs11808092(A;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position92607671
GeneEVI5
is asnp
is mentioned by
dbSNPrs11808092
dbSNP (classic)rs11808092
ClinGenrs11808092
ebirs11808092
HLIrs11808092
Exacrs11808092
Gnomadrs11808092
Varsomers11808092
LitVarrs11808092
Maprs11808092
PheGenIrs11808092
Biobankrs11808092
1000 genomesrs11808092
hgdprs11808092
ensemblrs11808092
geneviewrs11808092
scholarrs11808092
googlers11808092
pharmgkbrs11808092
gwascentralrs11808092
openSNPrs11808092
23andMers11808092
SNPshotrs11808092
SNPdbers11808092
MSV3drs11808092
GWAS Ctlgrs11808092
GMAF0.1478
Max Magnitude0
? (A;A) (A;C) (C;C) 28


[PMID 20087403OA-icon.png] Tag-SNP analysis of the GFI1-EVI5-RPL5-FAM69 risk locus for multiple sclerosis


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



ClinVar
Risk rs11808092(A;A)
Alt rs11808092(A;A)
Reference Rs11808092(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene EVI5
CLNDBN not specified
Reversed 0
HGVS NC_000001.10:g.93073228C>A
CLNSRC
CLNACC RCV000455680.1,