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rs4704970

From SNPedia

Orientationplus
Stabilizedplus
Make rs4704970(A;A)
Make rs4704970(A;G)
Make rs4704970(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position156073982
GeneSGCD
is asnp
is mentioned by
dbSNPrs4704970
ebirs4704970
HLIrs4704970
Exacrs4704970
Varsomers4704970
Maprs4704970
PheGenIrs4704970
hapmaprs4704970
1000 genomesrs4704970
hgdprs4704970
ensemblrs4704970
gopubmedrs4704970
geneviewrs4704970
scholarrs4704970
googlers4704970
pharmgkbrs4704970
gwascentralrs4704970
openSNPrs4704970
23andMers4704970
23andMe allrs4704970
SNP Nexus

SNPshotrs4704970
SNPdbers4704970
MSV3drs4704970
GWAS Ctlgrs4704970
GMAF0.1107
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19010793OA-icon.png]
Trait Multiple sclerosis (age of onset)
Title Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
Risk Allele
P-val 0.000007
Odds Ratio NR NR



GET Evidence
rs4704970
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.140625
summary