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rs11957313

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs11957313(A;A)
Make rs11957313(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position170523390
GeneKCNIP1
is asnp
is mentioned by
dbSNPrs11957313
ebirs11957313
HLIrs11957313
Exacrs11957313
Varsomers11957313
Maprs11957313
PheGenIrs11957313
hapmaprs11957313
1000 genomesrs11957313
hgdprs11957313
ensemblrs11957313
gopubmedrs11957313
geneviewrs11957313
scholarrs11957313
googlers11957313
pharmgkbrs11957313
gwascentralrs11957313
openSNPrs11957313
23andMers11957313
23andMe allrs11957313
SNP Nexus

SNPshotrs11957313
SNPdbers11957313
MSV3drs11957313
GWAS Ctlgrs11957313
GMAF0.1983
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 0.000009
Odds Ratio NR NR



GET Evidence
rs11957313
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.203125
summary