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rs299175

From SNPedia

Orientationminus
Stabilizedminus
Make rs299175(C;C)
Make rs299175(C;T)
Make rs299175(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position55802162
GeneNLRP11
is asnp
is mentioned by
dbSNPrs299175
ebirs299175
HLIrs299175
Exacrs299175
Varsomers299175
Maprs299175
PheGenIrs299175
hapmaprs299175
1000 genomesrs299175
hgdprs299175
ensemblrs299175
gopubmedrs299175
geneviewrs299175
scholarrs299175
googlers299175
pharmgkbrs299175
gwascentralrs299175
openSNPrs299175
23andMers299175
23andMe allrs299175
SNP Nexus

SNPshotrs299175
SNPdbers299175
MSV3drs299175
GWAS Ctlgrs299175
GMAF0.4137
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19010793OA-icon.png]
Trait Multiple sclerosis (severity)
Title Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
Risk Allele
P-val 0.000004
Odds Ratio NR NR



GET Evidence
rs299175
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.320312
summary